The FELIX program can directly read seven specific data formats: the old FELIX format, the new FELIX format, an ASCII format, and the FELIX for Windows FID format, Bruker FID or SER format (from AMX and newer models; parameter files must be in ASCII format), the Varian FID format, and JEOL ALPHA and LAMBDA. All other spectrometer data must be converted to one of the first three formats before FELIX can access it. For conversion the new format is the preferred choice. When compared with the old format the new format has the advantage that data can be moved between systems with different byte ordering without a problem. The ASCII format is generally only used when no other method of data conversion is available.
FELIX also includes several built-in data filters for common spectrometer data formats. These built-in filters all convert data to the FELIX new format. The following built-in data filters are available:
First you must make sure that FELIX can access the spectrometer data on disk. One option is to remotely mount the spectrometer data disks so that they are accessible to the workstation running FELIX. If this is not possible, then you must transfer the data from the spectrometer computer to the FELIX workstation. This is usually accomplished by using ftp to transfer the data via Ethernet.
All of the data filters require that the spectrometer data files be kept in their native form. For example, the X32 data filter for Bruker data expects to see the same file and directory structure that exists on the spectrometer. The Bruker "data file" is actually a directory containing subdirectories with experimental and processed data files. When the spectrometer data is transferred to the FELIX workstation, this entire directory structure must remain unchanged.
One way to assure that the directory structure remains unchanged is to first make a tar file of the desired data directories on the spectrometer. This tar file can then be transferred to the FELIX workstation using ftp in binary mode.Note:
Once the data have been transferred, you can untar the data to recreate the same directory structure as existed on the spectrometer.
Once the data files have been transferred to the FELIX workstation with the original directory structure, they are ready to be converted. The conversion process is basically the same for all types of data (1D, 2D, 3D, etc.). The data filters read the spectrometer-format data files and parameters and then create a new FELIX-format data file. This new file (which is often given the extension .dat) can then be directly read by FELIX.
To start the data-conversion routines, select the File/Convert/Data menu item. A pullright appears, listing the different spectrometer data formats that FELIX can convert. Once you select the specific type of spectrometer data from the pullright, a control panel appears which asks you for information about the location and name of the input and output data files.
For the input data you specify the name of the Input File to convert. This Input File can be an individual file (as for Bruker Aspect data) or a directory (as for Bruker X32 or Varian data). When the data consists of a directory of information (as for Bruker X32 data or Varian data) then the Input File is a directory name containing the spectrometer data to be converted. You specify the location of the Input File by entering the relative or absolute path in the Data Prefix box. Be sure to include a trailing slash in the path designation for a directory. The Data Prefix is prepended to the Input File name to specify the exact location of the data. If the Input File is located in the current directory, then you can set Data Prefix to "./".
For output data you need to specify both the Output File and the Data Prefix. The Output file is the name of the new-format FELIX file to be produced. This file is often given a .dat extension to identify it as a FELIX data file. As with the Input File, the Data Prefix specifies the location of the Output File to be written. Once again, be sure to include the trailing slash in the Data Prefix.
Note that Bruker X32/DMX data has a directory structure in which multiple experiments and processed data sets can be stored under the same filename. To indicate which set of experimental and processed data you want to convert, you need to specify a number for both the Experimental and Process data subdirectories. This number is an integer that indicates the name of the Experimental and Process data subdirectories you want to use for the conversion.
The last thing to specify when converting data is whether you want to byte swap the input data. If the spectrometer computer and the workstation computer use different byte orderings, then set the Byte Swap Input Data parameter to on. This would needed if, for example, the data were collected on an X32 computer and then transferred to an SGI computer for analysis. If the spectrometer computer and the workstation computer have the same byte ordering, then set the Byte Swap Input Data parameter to off. This would be needed, for example, between an SGI/DMX computer and an SGI workstation. If you are not sure how to set this parameter, try both settings. The incorrect setting will produce an error message or an FID that looks like noise. The correct setting should produce a valid-looking FID. Once you have determined the correct setting, you can use it for all subsequent transfers between the same spectrometer/computer combination.
The procedure for converting data is the same for 1D, 2D, and ND data. For each, a single new-format FELIX data file is produced. For 2D or ND data, the file produced contains multiple 1D data files.
Once the converted datafile is produced, it can be directly read into FELIX. The datafile should then be checked to make sure that it can be read properly by FELIX and that the referencing information is correct.
You can check the datafile by reading it using the File/Open menu item. If you set the file Dimension to 1D, then each time you read the data, FELIX loads the first datafile from the multidimensional data set. If you set the file Dimension to ND, each time you read the data, FELIX loads the subsequent datafile in the multidimensional data set. For 2D and ND data, it is a good idea to check at least the first few data blocks to make sure the data were converted properly.
A conversion filter can be used to convert processed data directly to the FELIX matrix format. This action can be accessed with the File/Convert/Matrix menu item. Currently, you can convert NMRPipe, NMRCompass, Bruker 2rr and 3rrr files, and Varian data. The resulting FELIX matrix file can then be directly accessed by the FELIX program.
You can import processed Varian spectral data (that is, phase files) into FELIX. These phase files can be for 2D or 3D data sets. Using a macro called sv2dpf, you create a parameter (.par) file corresponding to 2D processed data sets. Similarly, using a macro called sv3dpf, you create a parameter (.par) file corresponding to 3D processed data sets. Each of these macros is provided below, and both must be run by VNMR (that is, Varian processing software). These two macros are located in the FELIX gifts/VARIAN/matrix/ directory and must be transferred to the VNMR macro library directory before they can be run by VNMR.
When you specify that you want to import a Varian spectrum and provide the filename for that spectrum, FELIX automatically searches for a corresponding .par file and converts the data in that file into FELIX matrix format. If FELIX does not find a .par file with the same root name as the spectrum filename that you specified, the application displays a dialog box and prompts you to enter the spectral parameters manually.
If you are importing a 2D spectrum, you must rename the phase file to a name that corresponds to the root name of the .par file. For example, if you use the sv2dpf macro to create a file called test.par, you must rename the phase file to test.
The sv2dpf macro is as follows:
You use the sv3dpf macro to create phase files corresponding to different planes (f1f2, f2f3, f3f1) in a 3D data set. You generate the .par file corresponding to each plane by using the sv2dpf macro (described above). The sv3dpf macro is as follows:
As described earlier, each macro creates a parameter (.par) file. Keep in mind that the name of this file must correspond to the name of the spectrum that you want to import. The following table lists the contents of the .par file:
You need not have a fourth line in the .par file to import a Varian spectrum. However, you can add this line if either flags to define spectral zooming or the range of ppm along the tier dimension for 3D data appears.
According to VNMR convention, the format of the .par file is as follows. The order of the values in the first three lines of the .par file varies, depending on which set of planes is being read. That is:
1. For sv3d-generated f1/f3 planes (where f2 is the tier dimension):
2. For sv3d-generated f2/f3 planes (where f1 is the tier dimension):
3. For sv3d-generated f1/f2 planes (where f3 is the tier dimension):
A space is used as a delimiter in all the examples. You should also be aware that, because only a few pulse sequences use the second and third channel for the f1 and f2, respectively, the location of dfrq and dfrq2 will rarely be in the correct position. Therefore, you will need to add the correct spectrometer frequency. You can use the axis parameter in VNMR to determine the correct spectrometer frequency for all three axes.
In addition to the above choices, several gift filters are supplied with the software. These filters, which are not supported by Accelrys, are in the $BIOSYM/gifts/felix directory. For more information about these programs, see the README files in the various directories and see also Appendix C, Data transfer and conversion.
FELIX includes a quick-access menu that is connected to the right mouse button. This menu is intended to be your major customization point. (It is possible to rewrite the whole user interface, but just changing this menu and macro will allow your favorite commands to be easily accessible.) The necessary changes are described here. You need to copy the following file into your working directory to customize the macro connected to right mouse button:
mouser NULL NULL NULL NULL NULL NULL mouser.mot
You can change the last line from mouser.mot, to e.g.:
Then, in your current working directory, you can create a new file called mymouser.mot. For the sake of example we create a right mouse macro with the first item to draw a 1D file and the second, third, and fourth items to define the plotting parameters:
For those FELIX users who have also licensed the Insight II and NMRchitect programs, several features and capabilities allow FELIX and the Insight II/NMRchitect programs to interface with each other as seamlessly as possible. These features simplify the sharing of data between the programs and give you functionality that goes beyond what is available in either of the programs by itself. This task outlines the capabilities of the FELIX-Insight II interface and explains how to use these features to improve your productivity.
The FELIX-Insight II interface capabilities encompass three general categories: starting FELIX automatically from within the Insight II/NMRchitect program, sharing data between the two programs, and using the Insight II environment to display molecule structures. Each of these capabilities is discussed more fully below.
When both FELIX and Insight II are running on your computer, each has a display window open on your screen. To switch from one program to the other, simply mouse click on a window's header to pop that window to the front.
The communication between the two programs is in the form of a client/server model of two separate processes. FELIX and Insight II can pass commands and information back and forth as if they were one program. This capability is based on the UNIX inter-process communication (IPC) facility and the remote procedure call (RPC) interface developed by SUN Microsystems. As a result of this design, both FELIX and Insight II can issue commands and/or request information from each other. This allows you to more fully exploit the features of both programs at the same time.
At program start-up, both FELIX and Insight II automatically attempt to establish a socket connection, which can be thought of as a channel for communication between the two programs. A limitation of this UNIX facility is that the connection is always made for the first instance of each program currently running on that computer. This means that if another user in your group is already running FELIX on the same machine on which you start up Insight II and FELIX, then Insight II makes the socket connection to the other user, because his FELIX socket request was made before yours. To assure an appropriate connection between FELIX and Insight II, first make sure no one else is running either program on your computer when you start your session. Once the socket connection is made, other users may run additional copies of the FELIX and/or Insight II software without disrupting your connection.
You can start FELIX manually as a standalone program, or you can treat FELIX as a module of the Insight II/NMRchitect software package. To start FELIX from within Insight II, click the Accelrys logo (top left corner of the Insight II interface) and select NMR_Refine from the resulting list. Once you are within the NMR_Refine module, select the FELIX/Start_FELIX menu item. After verifying that you have selected the correct executable file and that the directory you want to run FELIX from is listed in the resulting control panel, select Execute. This starts FELIX, opens the FELIX graphics window, and begins the FELIX session.
The socket connection between the two programs works differently in some cases, depending on whether FELIX has been started separately or from within Insight II/NMRchitect. The Insight II/NMRchitect program can connect to FELIX only if FELIX is started from within Insight II/NMRchitect. FELIX, on the other hand, can connect to Insight II/NMRchitect whether FELIX is started separately or from within Insight II, as long as the NMR_Refine module is currently running.
Easy sharing of data between programs is one of the most important needs for two programs that interface together. Typically, not every single unit of data is needed equally by both programs. More often, only a few data sets need to be known by both programs, and often for rather dissimilar reasons.
For the FELIX and Insight II programs, three categories of data must be shared between the two programs: cross peak data, molecule coordinate data, and NMR-based molecule-refinement restraint data. Each of these data classes is stored and used differently by the two programs, yet all need to be passed back and forth as seamlessly as possible. Each of these data types and the manner of sharing them between FELIX and Insight II is discussed more fully below.
FELIX processes NMR data and searches the resulting matrices to find experimental cross peaks. Further analysis and assignment work yields cross-peak positions, widths, volume intensities, and atom assignments. All these types of information are stored in the FELIX database, which is designed for fast storage and searching of large complex data sets.
After FELIX has generated cross-peak information, you can export these data to the Insight II program for use by NMRchitect. Within Insight II, cross peak volume, assignment, and chemical-shift information is stored in four ASCII files:
To export cross-peak data from FELIX to Insight II, select the File/Export/Restraints menu item. This opens a control panel that asks you for information about the FELIX database: the matrix name, peak entity, volume entity, and scalar entity; the directory where Insight II files will be written; and the names for these new files. Since FELIX stores cross peaks in data-point units and Insight II uses ppm and Hertz, you must make sure the matrix is referenced. Performing this action creates three or four new ASCII files in the specified directory, depending on whether a restraint entity is present in the FELIX database. To read these files into Insight II, you select the FELIX/Read_From_FELIX menu item from within the NMR_Refine module.
After you have read the FELIX database into Insight II, the NMR_Refine module puts a Read_From_FELIX icon in the upper-left corner of the Insight II window. Clicking this icon performs subsequent FELIX/Read_From_FELIX actions using the same entity, file, and project names that you previously specified. This icon is useful for passing cross-peak data back and forth between the two programs, as it automatically performs both halves of the data transfer; first exporting FELIX database files, then reading those files into NMRchitect, all in a single step (with no control panels to fill in).
In addition to passing cross peaks from FELIX to Insight II, you can also move cross-peak data from Insight II to FELIX. These data may be either from experimental peaks originally generated by FELIX or from theoretical peaks generated by NMRchitect.
To create cross-peak files with NMRchitect, select the FELIX/ Write_To_FELIX menu item from within the NMR_Refine module. To read these ASCII files into FELIX, you next select the File/Import/Restraints menu item in FELIX. This opens a control panel that asks you for file and directory names for the files to be read in and for a matrix name and entity names for storing these peaks in the FELIX database.
After you have transferred the Insight II database to FELIX, the NMR_Refine module puts a Write_To_FELIX icon in the upper-left corner of the Insight II window. Clicking this icon performs subsequent FELIX/Write_To_FELIX actions using the same entity, file, and project names you previously specified. The icon is useful for passing cross-peak data back and forth between the two programs, as it automatically performs both halves of the data transfer in a single step: exporting NMRchitect database files and reading those files into FELIX (with no control panels to fill in).
To read Insight II coordinates into FELIX, the Model module must be licensed. Model is a separate option of FELIX that is not part of the standard release. If you need additional information on licensing the Model module, you should contact Accelrys (see the Accelrys System Guide). The Model module is accessed by selecting the Model menu item. If you do not see the Model item on the menubar, then you are not licensed for Model. You can read in a molecule in either InsightII format (.car or .mdf file is required) or in X-PLOR PDB format. The atom names of a molecule read into FELIX are preserved as Insight II type names. Thus, when building FELIX database information from scratch, you should use the Insight II naming convention. This is especially true if the database assignment information is going to be used for direct comparison with molecule structures.
For more information about Model, please see Chapter 6, Model interface.
To read and display IRMA intensities with Model, make sure you have a valid spectrum and select the File/Import/Theoretical menu item. A control panel appears, which asks you for the .pks, .ppm and .asn files that correspond to IRMA-generated data. The default values in the control panel are set when data is passed from Insight II to FELIX. This procedure is exactly the same as that for reading experimental cross-peak information from the Insight II database. When importing Insight II files into FELIX, you must specify a reference matrix. In addition, you must indicate which peak and volume entities to use for storing cross-peak information within FELIX. You can access and display the IRMA files by selecting the Model/Draw Theoretical menu item and entering names for the cross-peak and volume entities where the theoretical NOE data are stored.
After loading the FELIX database with the appropriate entities, the data must be scaled to match the experimental cross peaks for direct comparison - the program will ask you for a scalar peak or you can use later the Model/Set Scale menu item. This asks you for an unique assignment name or you can use the cursor to select a cross-peak footprint, which must be in both your experimental database and your back-calculated database.
For a more detailed description of the Model module, please see Chapter 6, Model interface.
One of the important types of data generated by FELIX is NMR-based restraints, which can be used as input to structure-determination studies of molecules. FELIX can produce NOE volume restraints, NOE distance restraints, 3J dihedral restraints, overlapped (ambiguous) NOE distance restraints, and overlapped (ambiguous) NOE volume restraints. Because all of these are used by NMRchitect for structure refinement, it is essential that Insight II and FELIX share these files.
FELIX reads and writes .rstrnt files as part of the actions that transfer data between the two programs. Every time cross-peak information is shared between FELIX and Insight II, all restraint information is also shared.
Insight II uses an ASCII file to store restraints, and FELIX uses a set of database entities. When FELIX imports restraints from Insight II, it creates entities to store them. If FELIX is used to generate NMR-based restraints, these are also stored in database entities. When FELIX exports restraints to Insight II, it writes all the restraint entities to a new .rstrnt file, which is then read into Insight II. All restraint categories are preserved during this sharing of data between the two programs.
You use the Measure/DISCOVER Restraints or Measure/X-PLOR Restraints menu items in FELIX to calculate NMR restraints and to create entities of volumes (NOE-intensities), distances, and 3J dihedrals. If you then export the FELIX database to Insight II, you are ready to do structure generation or refinement against those NMR restraints using NMRchitect.
The FELIX Model module performs calculations and generates displays of both NMR data and a molecule simultaneously. This includes the back-calculation of theoretical NMR data from coordinates and the interrogation of interatomic distances based on cross-peak intensities and assignments. FELIX provides this functionality by using multiple graphics frames to display experimental NMR data, theoretical NMR data, and the molecule. See Chapter 6, Model interface, for more information about the FELIX Model module.
Since FELIX is an NMR processing software package, it is understandable that its molecule display and analysis capabilities are rather primitive. For this reason, FELIX is set up to perform all molecule display and analysis in the Insight II program, while keeping the NMR display and analysis within FELIX.
The Model/Setup/Connect menu item can be used to toggle the Insight II window for molecule display. The controls in Model work as described in Chapter 6, Model interface, but all actions that display or analyze molecule coordinates are performed by Insight II and appear in the Insight II window instead of the FELIX window. This gives you seamless access to the more advanced molecule-rendering features of Insight II, using FELIX for NMR display and analysis and NMRchitect for NMR-based structure determination. Working together, these software tools provide more functionality than either program by itself.
FELIX provides a comprehensive set of tools for processing, displaying, and analyzing NMR data. This section outlines ways to use the menu interface for processing and analyzing your one-dimensional (1D) NMR data. For information on converting your data files into a format that can be read by FELIX, please see Task: Importing data, and Appendix C, Data transfer and conversion.
FELIX reads two distinct file formats of its own; and you must tell the program what format your data is in for it to be interpreted correctly. The `old' FELIX data format (the format that is read using the re command) is the format that most of the current public-domain and commercial reformatting programs generate. Although this data format works perfectly well on any given computer, data of this type cannot always be transferred between different types of computers due to byte-order differences. The new format was designed to provide increased portability for FELIX files (use the rn command to read these files). Files written in the new format can be transferred via ETHERNET without conversion.The built-in FELIX data filters create all new-format files.
FELIX can also read native spectrometer data formats via a set of new commands: rf for reading FELIX for Windows FID files, rb for reading Bruker FID or SER files, rv for reading Varian FED files and rj for reading JEOL ALPHA .nmf files and LAMBDA .nmfid files.
To read a data file, use the File/Open menu item. You can specify the data as either one-dimensional or N-dimensional, and as either Bruker, Varian, FELIX For Windows, JEOL, or FELIX old or new format. If you define the data type as one-dimensional, the data file is explicitly closed before it is read, to reset the record pointer to the first record. When you are first working with N-dimensional data, the program reads the first record from the serial data file. Each subsequent read (during the same FELIX session) increments the record pointer by one and reads the next data record.
As an example of reading in a sample data file, copy the 1D data file sample.dat from the $BIOSYM/tutorial/felix directory to your working directory. This file is accessible on your system only if the gifts and tutorial files were installed during FELIX installation. Otherwise, you must either copy the files you need directly from the gifts and tutorials CD or do a new installation, this time installing the gifts and tutorial files for FELIX. Once you have copied the sample data file to your working directory, try reading it into FELIX using the File/Open menu item.
In some instances, you might want to save the data to disk as a permanent record. For example, you can save a fully processed spectrum to a file so you can display it quickly without re-transformation. To do this, you select the File/Save As menu item. You must supply a file name: the data are saved in FELIX new format. If the file already exists, you are asked whether to quit or overwrite the file.
The most common way of manipulating displays is to use the View pulldown. View contains a set of menu item designed to manipulate the display of 1D data. For example, to redraw the current workspace, select the View/Plot menu item.
By default, when FELIX initially reads and displays a new file, it draws all the data points (the entire spectral width). To display or work with an expanded region of the spectrum, you must select the expansion limits as described below.
The View/Limits/Set Limits menu item allows you to choose spectrum limits in real time. When you select this menu item, a crosshair cursor appears. Move this cursor to the region you want to expand, push and hold down the left button on your mouse, drag out the region to be expanded, and then release the mouse button.
Alternatively, you can use the icons - particularly the Zoom icon - to execute this task.
FELIX control panels enable you to tailor the appearance of your data plots by showing the current settings for the plot appearance and permitting the settings to be changed. These control panels are accessed from the Preference/Plot Parameters menu item or by using the Plot Parameters icon.
FELIX allows and enhances processing and analysis of one-dimensional and N-dimensional spectra through the availability of additional addressable memory locations. These storage spaces are called buffers and may be used to temporarily save data. The data stored in the buffers may be as simple as a single data value or as complex as a protein spectrum. The FELIX buffers are addressed by number: buffer 1, buffer 2, ... buffer n. The size and number of buffers available is determined by the amount of memory configured for this use. The Preference/Memory menu item allows you to change the program's memory allocation. For example, if four 1D buffers are defined, each having a buffer size of 16384 complex points, enough space can be reserved to let you work with the current data plus four buffers for data containing up to 16384 points.
Buffers are accessed with the Tools/Buffers menu item. For example, to store the current information to a buffer, select the Tools/Buffers/Store Work to Buffer menu item and enter the buffer number in the control panel. To visualize this information, you must change the stack depth to include the buffers that you want to visualize. The Tools/Buffers menu item contains many additional controls that allow you to manipulate the contents of the buffers.
The stacks and buffers are generally used for displaying multiple spectra simultaneously. The stack represents the range of buffers selected for display. The View/Plot menu item shows all the data in the stack. This function draws the workspace first, followed by each item in the stack, from top to bottom or from bottom to top, based on the Stack Order parameter. The stack can be used to display several spectra along the same axis. By default, the spectra are scaled equally to use the space available along the y-axis. The Stack Overlap parameter can be used to set the display to no overlap (0), full overlap (1), or any fraction thereof. The Stack Depth parameter controls how many buffers in addition to the workspace are displayed when data are redrawn. The various stack parameters (Depth, Order, and Overlap) can be changed in the PLOT PARAMETERS - BASIC control panel, which is accessed by selecting the Preference/Plot Parameters menu item or the Plot Parameters icon.
The Absolute Intensity parameter also affects the appearance of the stack display. This parameter is used to set the scale factor for all data in the window to the same value, so that data intensities can be compared directly. When this parameter is set to No, all data in the stack are scaled to fill the available space. If this parameter is set to Yes, all data are scaled to the last spectrum drawn in the workspace. This switch is useful for displaying difference spectra, where the full spectrum and the difference can be compared on the same scale.
FELIX can display a spectral axis with several types of labels. The default axis label is points, because reliable point positions do not change when the values for the spectrum width and spectrometer frequency change. Axis units may be changed with the Preference/Plot Parameters control in the Scale control panel. Choices for the Axis Units parameter are None, Points, Hertz, PPM, Seconds, and 1/cm.
To reference a one-dimensional spectrum, select the Preference/Reference menu item, which asks you for the referencing information using the REFERENCE 1D DATA control panel. The Spectral Frequency and Spectral Width parameters must be set to the values of the spectrometer frequency in MHz and the spectrum width in Hz. You can enter the Reference Point value either by typing it in the box on the control panel or by clicking the Cursor button in the control panel. This causes FELIX to display a vertical cursor, which you move to the desired reference point on the plot and then click the left mouse button. At this time the REFERENCE 1D DATA control panel reappears. Now enter the reference value in the appropriate box - for axis units of Hertz enter a reference value in the Reference Hertz box, for ppm units enter a reference value in the Reference PPM box. When you are finished, select OK to close the control panel and redisplay the data with the selected axis units.
The Measure/Cursor Position menu item allows you to obtain point numbers, ppm values, and corresponding data values. When you select the Measure/Cursor Position menu item, a vertical cursor appears, which updates the current axis position and data value when you move it with the mouse. The axis position is in axis-based units - if your axis is in points it tracks in points, if your axis is set to ppm it tracks in ppm. To quit the cursor-tracking mode, press <Esc>. The data value shown is the actual data value stored at that location in the workspace.
When you are displaying data in several frames at once, you may sometimes want to use the mouse to point to the same data-point values in all the frames simultaneously. FELIX provides correlated cursors for this purpose. Correlated cursors are multiple crosshair cursors that track in more than one frame; for example, if there are three frames, three crosshair cursors track the mouse motion. The center of each cursor falls on the same data point value in each frame. You can turn on correlated cursors by selecting the Measure/Correlated Cursors menu item. To find the cursor position and data-point value, click the mouse button. To quit the correlated-cursor mode, press <Esc>.
In addition to spectrum positions and intensities, you can calculate the separation between any two spectrum features in a display with the Measure/Distance/Separation menu item. You use a crosshair cursor to select two locations on the display. FELIX reports the separation in points, ppm, and Hertz. To quit this mode, press <Esc>.
Zero-filling is a common manipulation performed on time-domain data. By selecting the Process1D/Zero Fill menu item, you can increase the number of points in the transformed spectrum, and thereby increase the spectrum's apparent digital resolution. Raw FIDs are usually corrected prior to Fourier transformation, to remove any DC offset that may have occurred during data acquisition. This is done by selecting the Process1D/DC Offset menu item. You can select regular BC (baseline correction) or DBC (for Bruker oversampled data) and set a Baseline Correction Fraction. The Baseline Correction Fraction specifies the fraction of the FID, starting from the right side, to be averaged to eliminate the DC offset.
Linear prediction estimates the value of a point based on the values of adjacent points and can be used to replace corrupted values in an FID. Often, several of the first data-point values can be corrupted by instrumentation-induced artifacts. Therefore the spectrum can be noticeably improved when these corrupted point values are replaced with values estimated by linear prediction, where the estimated values are based on subsequent points - points of greater integrity.
A second application of linear prediction to NMR data is to extend an FID. This is useful for experiments in which the data collection stopped before the signals completely decayed; that is, the FID is truncated. Here, the data values of the FID are used to estimate new data values that are appended to the end of the FID.
The Process1D/Transform/Linear Prediction command is used to replace data values at the beginning of the FID. In the control panel that appears, you indicate the Points to use in the predication (the points that are used to calculate the coefficients) the Number of Coefficients, and the Number of Peaks. The Points to use defines the number of points used to calculate the LP coefficients. The Number of Coefficients specifies the number of LP coefficients that are calculated. The Number of Peaks is there for compatibility with existing macros, but is not used in the current LP implementation.
The length of time taken by an LP calculation is determined in large part by the number of data points that are used to determine the LP coefficients. In general, the quality of the LP calculation also increases with the number of data points used in the calculation. It is therefore necessary to pick a value for the Points to use that is large enough to produce accurate predicted data values but that does not unduly lengthen the time taken by the LP calculation. The value for the Number of Coefficients is generally set to be one-quarter to one-third of the Points to use.
The Process1D/Transform/Linear Prediction command is also used to replace data values at the end of the FID and can also be used to extend the FID. Conventional linear prediction works well when the data are being extended by a small fraction of the number of points. However, when the number of data points is being extended by a large fraction (e.g., doubling the number of points), the predicted data can contain signals with increasing amplitude due to the effect of noise on the predicted LP coefficients. The net effect can be an FID with increasing (as opposed to decreasing) amplitude as a function of time. To prevent this, FELIX allows the option of using Root Reflection when predicting data. Root Reflection ensures that the calculated frequency components decay as a function of time and thus more accurately reflect the correct physical nature of an FID. Using Root Reflection increases the time needed to perform the LP calculation, but the predicted points are more representative of a true FID. Root Reflection is essentially required when predicting large numbers of data points, to avoid having noise components with increasing amplitude dominate the predicted FID at longer time values.
FELIX allows great flexibility in how the LP calculation is performed. By default, the Process1D/Transform/Linear Prediction command is used for extending the data, but it also allows you to specify exactly which points you would like to use in the LP calculation and which points you would like to predict. The method used to perform the LP calculation is specified by you - the available choices are Forward, Backward, Forward-Backward, and Mirror Image. The Forward method of linear prediction is what was used in previous versions of FELIX. The Forward-Backward technique (Zhu and Bax 1992) performs both a Forward and a Backward calculation on the data. The resulting LP coefficients are then averaged to produce a more accurate set of LP coefficients than either the Forward or Backward method can produce alone.
The Forward-Backward method is very robust and generally applicable, and does not require any prior knowledge of the FID. Mirror Image linear prediction is a method by which predicted data at negative time values are used in the calculation. This technique allows more LP coefficients to be calculated and hence is useful for severely truncated data. When you use the Mirror Image technique, you can increase the Number of Coefficients to between one-half and two-thirds the value of the Points to use. The Mirror Image technique requires prior knowledge of the phase of the data and nondecaying signals. Because of these restrictions, the Mirror Image technique is used primarily for severely truncated indirect dimensions of N-dimensional data sets when there is a need to calculate more LP coefficients than would be possible with the Forward-Backward method. The Mirror Image method includes options for data collected with no sampling delay and data collected with a one-half dwell time sampling delay.
FELIX offers three methods for reducing the intensity of strong solvent signals - a linear-prediction-based algorithm, a convolution-based method, and a polynomial-based method. All three methods are accessible by using one of the options in the Process1D/Solvent Suppression menu item.
Linear-prediction-based solvent reduction is accessed by choosing Linear Prediction as the Method. With this technique, the LP algorithm is used to estimate and remove contributions from the most intense components in the spectrum. This technique works well when the intensity of the solvent signal to be removed is much greater than the other signals that are present.
Convolution-based solvent reduction is accessed by selecting Time-Domain Convolution from the Method popup in the control panel that appears when you select the Process1D/Solvent Suppression menu item. In this technique, a convolution is done to first identity the lowest-frequency components that are present, and then these components are subtracted from the data. This technique is very useful as long as the solvent signals to remove are present at the carrier frequency.
Polynomial-based solvent reduction is accessed by selecting Polynomial from the Method popup in the control panel that appears when you select the Process1D/Solvent Suppression menu item. In this technique, a polynomial is fitted to the data, and the resulting function is subtracted from the time domain data. This technique works best when the solvent resonance is close to zero frequency.
Time domain NMR data can be multiplied by window functions that perform digital filtering for the purpose of reducing noise or increasing spectral resolution. For example, the noise level in 1D NMR data can be attenuated by multiplying the FID by an exponential window function.
FELIX offers two methods for selecting window function parameters - you can enter the parameter values directly or you can adjust them interactively. The Process1D/Window Function menu item allows you to select a window function and adjust its parameters interactively while FELIX displays plots of both the window function and the product of the FID and window function. FELIX can also display the spectrum rather than the FID and window function product, while you adjust the window function parameters. This function is extremely useful in determining which window function is appropriate for your data.
You can also explicitly specify a window function and its parameters with this menu item. When you know exactly what window function you want to use, as well as its parameters, this action lets you apply it quickly and precisely.
Sinebell, Sinebell squared, Skewed sinebell, and Skewed sinebell squared windows are a useful (but potentially dangerous) family of apodization functions. These sinebell windows can be shaped in many different ways, depending on their size, phase, and skew. The basic sinebell window is simply the sine function from zero to p, mapped onto the number of points in the FID. If a spectrum is to be integrated following application of a sinebell window, a phase shift of 90° is the only honest sinebell to use, because the first point of the FID is not changed. The sine squared window has the advantage that it approaches zero smoothly, whereas the sinebell does not. Sinebell squared windows shifted 90° are useful for avoiding truncation effects when zero filling badly truncated data. The skewed sinebells are primarily useful for adjusting the line shapes of magnitude and power spectra when phase information has been lost.
|sinebell||sinebell squared||skewed sinebell||skewed sinebell squared|
Exponential linebroadening is the most commonly used window function. This function starts out equal to one at the first point and decays at the rate of the specified FID. Because the value of the first point in the FID is not changed, exponential windows do not alter integral intensities and are a good window to use if integrals are to be measured. Exponential windows allow you to trade line width for signal to noise but preserve the Lorentzian line shape. If you use an exponential window to reduce noise, be aware that the lines in the spectrum still have Lorentzian shapes but no longer have natural line widths. For more detailed information, please refer to the em command in the FELIX Command Language Reference Guide.
Gaussian linebroadening is another popular window that changes not only the line width, but also the line shape. Gauss/Lorentz multiplication modifies the value of the first point of the FID and hence the value of the integral. Gauss/Lorentz is commonly used for resolution enhancement and changes the line shape to be partly Gaussian. Gaussian lines have narrow tails and yield a nicer-looking spectrum. This window is appropriate for cosmetic resolution enhancement, but the line widths and line shapes are no longer natural. Gaussian multiplication also alters the integral of spectral lines and differentially reduces the integral of broad lines with respect to narrow lines. Although a spectrum with Gaussian line shapes looks great, you must use caution if you attempt to integrate it, since the integral is affected by the line shape. For more detailed information, please refer to the gm command in the FELIX Command Language Reference Guide.
The Kaiser window is a function by Hamming (1989). This window is useful for apodizing data that are truncated. For more detailed information, please refer to the kw command in the FELIX Command Language Reference Guide.
The Trapezoidal function multiplies the data in the workspace by a window that rises from zero at the first point to one at <p1>, is equal to one from <p1> to <p2>, and falls to zero from <p2> to <p3>. For more detailed information, please refer to the tm command in the FELIX Command Language Reference Guide.
The advantages of applying a pulse to the nuclear spins and collecting the resulting transient - advantages that range from improving the signal-to-noise ratio to making possible forbidden detection of multiple quantum coherence - have made this NMR technique predominate. The Fourier integral transform is central to modern NMR data processing because it transforms the transient from the time domain to the frequency domain, thereby yielding a spectrum.
Accordingly, FELIX provides a battery of Fourier integral transforms that are accessed by selecting the Process1D/Transform menu item, which opens a control panel containing a list of the integral transforms that FELIX can perform on the data in the work space. Five Fourier transforms and a Hilbert transform are on this list. The most commonly used transform method are listed below.
The Complex FFT method applies a complex Fourier transform to the data in the work space. For this transform, the data must be true complex data, characterized by simultaneous sample and conversion of the real and imaginary signals. This is the most common of the Fourier transform methods and is used for most data.
The Bruker FFT method performs a complex Fourier transform on complex data that is unique to some Bruker spectrometers. These spectrometers cannot sample and convert the real and imaginary signals simultaneously; instead, they collect the real and imaginary signals alternately. This is reflected in the acqus file when the AQ_mod parameter is set to 2. If your data were collected in this mode, you must use the Bruker FFT method.
The Oversampled FFT method performs a complex Fourier transform on digitally oversampled data collected on Bruker DMX series and newer spectrometers. If your data were collected using digital oversampling, you should use this method for the transform.
After Fourier transformation, a spectrum frequently appears to be out of phase - that is, the resonance lines appear to be a mixture of absorptive and dispersive shapes. This is due to several factors, including finite pulse lengths, acquisition delays, and analog filter response. NMR spectra can be phase corrected after transformation by multiplying each datapoint value pair by a phase factor.
FELIX has three different ways to apply phase correction to a spectrum, which are accessed by selecting the Process1D/Phase Correction menu item. The automatic phase-correction algorithms include the PAMPAS and APSL methods for spectra with non-split peaks, such as decoupled 13C and DEPT spectra, an algorithm based on peak integration for general in-phase 1D spectra, and a basic algorithm intended for common proton spectra. In addition to the automatic phase-correction routine, FELIX provides an interactive real-time phase routine that is easy to use. FELIX also allows you to enter the zero- and first-order phase parameters explicitly.
An NMR spectrum can exhibit substantial baseline distortions that arise from non-ideal experimental conditions. Such distortions can interfere with analysis of the spectrum, for example peak picking and integral calculation, so they must be minimized. Fortunately, most baseline distortions can be minimized easily, by first identifying a set of points on the spectrum that are free of peaks. These points are called baseline points. Next, a smoothly varying function is fitted to the set of baseline points. This function is expected to closely approximate the baseline distortion. Finally, at each point, the value of the smoothly varying function is subtracted from the data value in the work space, thereby removing the baseline distortion from the spectrum.
With the Process1D/Baseline Correction menu item, you can either add and delete baseline points or you can use different options to correct the baseline.
FELIX uses an integrated database for storing spectrum information, including the identities of selected baseline points. By default, the name of the baseline point entity is bas:baseline; however you can change this name. In fact, if you want to retain the baseline points stored in the current entity while you pick a new set of baseline points, you must change the entity name. To change the name of the current baseline point entity, select the Preference/Table menu item. To change the name, enter the name of a new or existing baseline point entity and select OK.
To view the contents of the baseline point entity, select the name of the entity in the Edit/Table menu item. This creates a table display of the baseline point entity contents in a separate window. You may add or delete baseline points on the spreadsheet.
At times you may want to save a baseline point entity in an ASCII file. This is done by selecting the File/Export menu item. You are asked for an output file name, as well as the name of the baseline entity to save. The ASCII file is written to the current directory or to the FELIX text directory, depending on how your directory structure is configured.
A baseline point ASCII file may be read into a baseline point entity by selecting the File/Import menu item. You are then asked for an input file name as well as an entity name.
When you are correcting the baselines of spectra, it is often necessary to test several sets of baseline correction points and functions before a spectrum can be satisfactorily corrected. This is especially true if it is difficult to define baseline points due to spectral crowding.
For this reason, we highly recommend that you save your spectrum by selecting the File/Save As menu item before applying any baseline-correction function. Then, if you are not satisfied with the results of any given baseline-correction function and its application to your data, you can select the File/Open menu item to read your saved spectral data in again.
Selecting the Process1D/Baseline Correction menu item opens a control panel containing the available choices for adding and deleting baseline points. First you have to toggle on the Baseline Points radio button.
To define the baseline points, select the Auto Pick Points or Auto Pick Points w/FLATT option from the popup. This automatically generates a list of baseline points. Markers for each baseline point picked in the spectrum are shown at the bottom of the current spectrum.
To add baseline points singly, use the Pick Points Via Cursor option. Move the crosshair cursor to baseline points, and click them with the left mouse button. To quit this mode, click outside of the spectrum. If you want, you may add baseline points explicitly using point numbers with the Manual Pick Points control.
If you make a mistake while selecting individual baseline points or if you want to modify the current list of baseline points, you can delete a region of points. Select the Delete Points in Region option in the Process1D/Baseline Correction menu item's control panel to create a small crosshair cursor. Then drag out a region of baseline points to delete.
To delete all the baseline points, select the Delete All Points option. This deletes the current baseline points entity from the database: it requires confirmation via a dialog box.
Once the baseline points are defined, you can choose a baseline-correction algorithm. The cubic spline algorithm, applied by setting the Baseline Correction to Cubic Spline in the control panel for the Process1D/Baseline Correction menu item, generates a baseline that passes exactly through each baseline point. A cubic spline may yield a kinked baseline if the defined baseline data points are close together and noisy.
The polynomial baseline correction algorithm generates smoother baseline correction functions from baseline points. This baseline correction is applied by setting the Baseline Correction to Polynomial in the control panel for the Process1D/Baseline Correction menu item. The polynomial correction differs from the cubic spline correction algorithm in that the baseline does not necessarily pass exactly through each baseline point, but a best fit is calculated.
The FELIX real-time baseline correction feature lets you adjust the coefficients of a polynomial baseline function while displaying the resulting baseline function superimposed on the baseline-corrected spectrum. You access the real-time baseline correction feature by setting the Baseline Correction to Real-Time Polynomial in the control panel for the Process1D/Baseline Correction menu item.
The above baseline-correction methods require that a set of baseline points already exist. In contrast, the three baseline correction methods below do not need pre-defined baseline points. Instead, they themselves determine what constitutes the baseline.
One of the baseline-correction functions supported by FELIX that does not require explicit baseline points is applied by setting the Baseline Correction to Automatic w/abl in the control panel for the Process1D/Baseline Correction menu item. This automatically selects noise points and performs a baseline correction for each point. The method involves the DC convolution of baseline points with a moving average, while applying a straight-line correction to non-baseline intervals (Dietrich et al. 1991).
FELIX also provides the FLATT baseline-correction algorithm (Güntert and Wüthrich 1992), which automatically finds baseline segments in the spectrum and uses a linear least-squares solution to fit a truncated Fourier series to these points. To use FLATT, set the Baseline Correction to Automatic w/FLATT in the control panel for the Process1D/Baseline Correction menu item.
The third baseline-correction function that does not require explicit baseline points is based on FaceLift, a technique introduced by Chylla and Markley (1993). The FaceLift algorithm automatically identifies base points from peak signals. To use FaceLift, set the Baseline Correction to Automatic w/FaceLift in the control panel for the Process1D/Baseline Correction menu item.
FELIX contains several menu items that affect frequency domain spectra in the workspace. Although most of these controls are directly related to the transformation of multidimensional spectra, several of them affect the processing of one-dimensional data. To access these tools, select the Tools pulldown.
Picking 1D peaks or resonances within FELIX is performed using the menu items within the Peaks pulldown.
FELIX uses an integrated database for storing spectrum information, including the identities of picked peaks. By default, the name of the 1D peaks entity is pic:1d_picks; however, you can change this name. In fact, if you want to retain the 1D picked peaks stored in the current entity while you pick a different set of peaks, you must change the entity name. To change or view the name of the current 1D peaks entity, select the Preference/Pick Parameters menu item. A control panel appears with the name of the current 1D peaks entity displayed in a the Peak Pick Table box. If you want to change the name, enter the name of a new or existing 1D peaks entity and select OK.
To view the contents of the 1D peaks entity, select the Edit/Peaks menu item. This action creates a spreadsheet display of the 1D peaks entity contents. You may add or delete 1D peaks on the spreadsheet, which also changes the information in the database.
At times you may want to save a 1D peaks entity in an ASCII file. This is done by selecting the File/Export/Peaks menu item. You are asked for an output file name, as well as the name of the entity to save. The ASCII file is then written to the current directory or the text subdirectory, depending on how the FELIX directory structure is configured.
A 1D peaks ASCII file may be read into a 1D peaks entity by selecting the File/Import/Peaks menu item. You are asked for an input file name as well as an entity name.
The first parameter you need to define before picking peaks is the threshold value. To do this, select the Preference/Pick Parameters menu item, set the Threshold Value to Cursor, and select OK. Move the cursor so that the horizontal half-crosshair is located at the level of the smallest peak you want to pick, and then click the left mouse button. The dialog box will appear with the newly set threshold. Accept it by selecting OK.
To automatically select peaks in the current display, select the Peaks/Pick All menu item.
To select peaks in a sub region of your display, select the Peaks/Pick Region menu item. This creates a small crosshair cursor that you may drag to select a picking region.
You may also select one peak at a time with the Peaks/Pick One menu item.
There are three options for deleting picked peaks. The Peaks/Remove All menu item actually deletes the 1D pick entity and the peak table and therefore removes all picked resonance information. The Peaks/Remove Region menu item is used to delete peaks in a region that you select by dragging the small crosshair cursor. You can delete peaks one-by-one by selecting the Peaks/Remove One menu item and clicking the peaks.
The Preference/Pick Parameters menu item displays a control panel listing those parameters that affect 1D peak picking. The threshold value can be inspected and set here. You can control the displayed names for picked peaks with the Peak Pick Units parameter. All peaks are displayed in Points, PPM, Hertz, or None. You can also display peak names on the peaks by setting the Peak Pick Units parameter to Assignment.
Three different peak-selection modes are provided. They are: positive peaks only, negative peaks only, and positive and negative peaks together. You can also vary the style of the peak markers, specifying arrowheads only, lines only, or lines with arrowheads.
FELIX offers a powerful line-fitting interface for deconvolution of complex spectra into individual peaks that are described by an analytic function of intensity, linewidth, and frequency. These functions allow precise integration of peaks individually.
The interface and display utilities are accessed by selecting the Peaks/Optimize menu item, which gives you access to the 1D line fitting function and other functions that display the actual data, the synthetic data, or residual data - either separately or all together in an overlay.
To fit a spectrum, select the Optimize option in the control panel associated with the Peaks/Optimize menu item.
Peak integration of a spectrum gives information about the relative number of spin species. Accurate integration is an important part of 1D data analysis. The integration options are accessed with the Measure/Integral/Volume menu item.Note:
FELIX allows you to integrate the entire spectrum either as a single integral or in shorter segments. To integrate the entire spectrum, simply select the View/Draw Integrals menu item. However, if current segments are defined, you must first select the Preference/Integral menu item and set the Integral Display Type option to Entire Spectrum.
FELIX uses an integrated database for storing spectrum information, including the identities of selected integral segments. By default, the name of the integral segment entity is seg:segments; however, you can change this name. In fact, if you want to retain the integral segments stored in the current entity while you pick a new set of integral segments, you must change the entity name. To change the name of the current integral segment entity, select the Preference/Table menu item. If you want to change the name, set the Table Type parameter to Integral Segments, enter the name of a new or existing integral segment entity, and select OK.
To view the contents of the integral segment entity, select the Edit/Table menu item and choose the segment entity. This creates a spreadsheet display of the integral segment entity contents. You may add or delete integral segments on the spreadsheet.
At times you may want to save an integral segment entity in an ASCII file. This is done by selecting the File/Export/Table menu item. You will be asked for the name of the entity (table) to save, as well as for an output file name. The ASCII file will be written to the directory selected in the file selection control panel.
An integral segment ASCII file may be read into an integral segment entity by selecting the File/Import/Table menu item. You are asked for an input file name and an entity name.
When integrating spectra, it is often necessary to try several permutations of integral segments and normalization before a spectrum can be integrated satisfactorily. This is especially true if it is difficult to define segments or baseline points due to crowding. Thus, FELIX provides keypad navigation tools to quickly change displayed regions, as well as the Slope and Bias option in the control panel belonging to the Measure/Integral/Volume menu item, which you can use for manipulating integrals in real time.
The Preference/Integral menu item is used to affect integral displays. Selecting Entire Spectrum as the Integral Type shows only the full spectrum. Selecting Segments, no values shows integrals only, with no integral values. Selecting Segments, values above displays integral values above the integrals, and selecting Segments, values below displays the integral values below. Selecting None turns off the display of integrals.
To define integral segments, select the Add Segment option in the control panel belonging to the Measure/Integral/Volume menu item. Integral segments are added by dragging out a segment region with the cursor. As long as you select a valid region within your spectrum, you can add additional segments without reselecting the Measure/Integral/Volume menu item. To exit this mode, click outside the spectrum.
If you make a mistake while selecting individual segments or if you want to modify the current list of segments, you may delete a small subregion of segments graphically. First, select the Remove Segment option in the control panel belonging to the Measure/Integral/Volume menu item to create a small crosshair cursor. Then drag out a region of segments to delete.
To delete all segments, select the Remove All Segments option in the Measure/Integral/Volume menu item. This action deletes the current integral segments entity from the database and requires confirmation via a dialog box.
For some spectra, it is impossible to accurately define baseline points. By selecting the Slope and Bias option in the control panel belonging to the Measure/Integral/Volume menu item, you can adjust these parameters in real time using sliders. If the baseline is significantly distorted, even adjusting the slope and bias may not be able to generate correct integral shapes. By adjusting the slope and bias, you are able to dial an integral value to anything you want. Thus, use these adjustments cautiously.
The Slope slider is used to adjust the integral slope parameters between -1 and 1.
The Bias slider is used to adjust the integral bias parameters between -1 and 1.
You may also adjust the integral slope and bias parameters manually using the Preference/Integral menu item.
FELIX enables you to normalize the integral of any segment of the spectrum to an arbitrary value. Four different normalization options are available via the Measure/Scalar/Normalize menu item. After normalization, the volume element in the integral segment entity is updated to the normalized value.
This section describes the general procedures for processing 2D data. For information on converting your data files into a format that FELIX can read, please see Task: Importing data, and Appendix C, Data transfer and conversion.
Multidimensional data are processed and stored by the FELIX program using matrix files. Matrix files are designed to allow easy access to and manipulation of the individual vectors that compose the data. In fact, virtually all N-dimensional processing is a repeated process of loading a vector from the matrix into the workspace, processing that vector, and then storing that vector back in the matrix. Therefore, the next step in multidimensional processing is to build a matrix file that will be used to hold the N-dimensional data.
Once a matrix file has been created, the individual FIDs that make up the FELIX data file are read in one by one, processed, and saved to the matrix file. Subsequent dimensions are processed by loading each vector in the given dimension one by one from the matrix into the workspace, processing each vector in turn, then storing the processed vectors back in the matrix file. This process is repeated for each dimension of the matrix.
In practice, these processing steps are generally carried out using macros. Macros are files that contain a series of instructions used to process the data. The FELIX program includes a very flexible macro language (FCL), which allows you to control all aspects of how the data are processed. You can use your own macros to process the data or to use the EZ macros. The EZ macros are a series of predefined processing macros that are intended to be used for the most common types of multidimensional data. In general, using your own custom macros is preferred, but the EZ macros will often be adequate.
The following macro shows an example of how to process the D1 dimension of a 2D data set. This sample macro is appropriate for either States or TPPI data. The line numbers are for reference only and are not included in the actual file.
3 def datfil `my2dfile.dat'
4 def matrix `my2dfile.mat'
5 def d1zfil 2048
6 def d2zfil 2048
7 def numd1 512
10 bld &matrix 2 &d1zfil &d2zfil 0 y
11 mat &matrix w
13 def temph0 -63.7941
14 def temph1 -130.5324
16 def datsiz &d1zfil
17 def datype 1
18 set 1
19 ss 2048 60
20 stb 1
22 ; D1 processing
24 ty D1(t2) Processing.
25 ty ---------------------
28 for row 1 &numd1
29 esc out
30 if &out ne 0 quit
31 rn &datfil
32 if &status ne 0 eof
33 def phase0 &temph0
34 def phase1 &temph1
35 def datype 1
36 bc 0.2
37 lpf 32 16 8 1
38 cnv 0 48
39 mwb 1
43 sto 0 &row
44 ty Row=&row $
47 if &status ne 0 then
48 def status 0
49 ty End-of-file on record &row
51 ty D1(t2) transform completed.
52 ty --------------------------------
55 def status 0
These lines define a series of symbols whose values determine how the data processing is to be performed. You do not need to define these symbols separately in the beginning of the macro. You can choose to enter processing-specific parameters on the individual command lines. However, grouping important symbol definitions at the beginning of a macro tends to remind you which parameter values may need to changed for different processing sessions.
The cmx command is used to close any open matrix files. Then the bld command is used to create an empty matrix file of the appropriate size. The zero in the bld command line indicates that the matrix to be created will be real. Most multidimensional data processing is done with real matrix files. The mat command is then given to open the matrix that was just created with write access.
These two lines define a pair of symbols (temph0 and temph1) which are used to store the zero and first-order phasing parameters. You need to store the desired phasing parameters in temporary symbols, because later, when the input data files are read in, the phase0 and phase1 symbols will be overwritten by the phasing values that were stored in the input data file.
This section of the macro illustrates how to set up an apodization function in buffer 1. Then later in the processing-loop section of the macro, each FID is multiplied by the contents of buffer 1. This is a more efficient method of doing the apodization compared to recalculating the appropriate apodization function for each FID. The first couple of lines define the datsiz symbol as the appropriate number of complex data points and the datype symbol as one that indicates complex data. The set command then sets all the real values in the workspace to 1. The appropriate apodization function is then performed and the result is stored in buffer 1.
These lines print out a message to the text window that the D1 processing loop is about to begin.
The cl command is used to close any open data file. This ensures that a subsequent read command (re or rn) will read the first record of the data file.
This section of the macro forms the main processing loop. This loop is executed once for each data file in the input data set.
These two lines of the macro show how the esc command can be used to allow you to interrupt a macro during execution. Such checking slows down the processing, so you may prefer not to use it. (Another way of stopping a macro's execution is to press the <Ctrl> and \ (backslash) keys together.) The esc command monitors keyboard input for the escape character. When the <Esc> key is pressed the user-defined symbol (in this case the out symbol) is set to one. An if statement transfers control out of the loop when the out symbol is no longer equal to zero.
These two lines read the next data set from the input data file and check the status of the read command. The re command is used to read old-format data and the rn command is used to read new-format data. If the read command is successful, the status symbol is set to zero. If the read command is not successful because, for example, you tried to read more data sets than were present in the input data file, then the status symbol is set to a non-zero value. If the read is not successful, then control is transferred out of the loop.
These two lines make sure that the phase0 and phase1 symbols, which are used by the subsequent phasing command (ph), are set correctly based on the saved phasing parameters (temph0 and temph1). This is necessary (as mentioned above) because, when a read command is given (re or rn), the phase0 and phase1 symbol values are overwritten with the phasing values that are stored in the input data file.
This line sets the datype symbol to one which represents complex data. This is required so that subsequent processing operations operate properly.
These are the main processing steps. The data are baseline corrected, the first point is corrected, and solvent is removed, apodized, ft'd, and phased. You would customize this section of the macro to correctly process your data. Apodization is performed by multiplying by buffer 1. Buffer 1 contains the apodization function that was set up earlier in the macro.
The data are then reduced so that only the real part of the FID is retained. This real data are then stored in the matrix. A type command (ty) is used to print out the current row so that you can monitor the progress of the macro. It is important to note that output to the text window is rather time consuming, and the processing can be sped up by 10-20% if you do not to use it.
If a read command should fail (such as by trying to read more input data sets than are present in the input data file) then control transfers to this section of the macro. A message is printed telling you on which record the failed read occurred.
If the macro finishes normally or you exit the macro early, then control transfers to this section. A cmx command closes the open matrix. The status symbol is set to zero, indicating a normal exit, and control is returned to the menu interface.
The following macro shows an example of how to process the D2 dimension of a 2D data set. This macro is appropriate for States data. This example assumes that 512 FIDs (256 complex points in D2) were collected in the D2(t1) dimension and that a real matrix was used with 1024 ¥ 1024 points. The line numbers are for reference only and are not included in the actual file.
3 def matrix `my2dfile.mat'
4 mat &matrix w
6 ty D2(t1) Processing.
7 ty ---------------------
9 for col 1 &d1size
10 esc out
11 if &out ne 0 quit
12 loa &col 0
13 def datype 1
14 def datsiz 512
15 zf 1024
16 ss 256 90
20 sto &col 0
21 ty Col=&col $
24 ty D2(t1) transform completed.
25 ty ------------------------------
The cmx command is used to close any open matrix files. Then the mat command is used to open the appropriate matrix file for writing.
This section forms the main processing loop. Since this macro operates on the D2 dimension, a column must be processed for each D1 point value. The for loop increments the symbol col from 1 to the value of the symbol d1size. When a matrix is opened, the value of the symbols d1size, d2size, etc. are set to the number of points in the corresponding dimension. Thus, the symbol d1size is automatically set to the number of points in the D1 dimension and is therefore a logical choice to use as the maximum value of the for loop.
These two lines of the macro show how the esc command can be used to allow you to interrupt a macro during execution. Such checking slows down the processing, so you may prefer not to use it. (Another way of stopping a macro's execution is to press the <Ctrl> and \ (backslash) keys together.) The esc command monitors keyboard input for the escape character. When the <Esc> key is pressed the user-defined symbol (in this case the out symbol) is set to one. An if statement transfers control out of the loop when the out symbol is no longer equal to zero.
The loa command is used to load the next column into the workspace for processing.
Since this is States data, the datype symbol is set to 1, indicating complex data. Now that the data are complex, the data size (datsiz symbol) must be reduced by half, because there are only half as many complex points compared to the number of points in the vector when it was first read in as real. If the data size is not reduced by half, then the second half of the workspace will contain invalid data. The data size is then doubled by zero-filling, so that the second half of the FID will contain zeros. The data size in complex points (datsiz) is now equal to the number of points in the D2 dimension of the matrix.
The data are then apodized, ft'd, and phased. The apodization is over 256 complex points. This is due to the fact that the 512 FIDs collected in the D2 dimension correspond to 256 complex points in D2. Because this is States data, a complex fit is performed.
The data are then reduced so that only the real part of the FID is retained. The data size (datsiz parameter) remains unchanged and is equal to the number of points in the D2 dimension of the matrix. These real data are then stored in the matrix. A type command (ty) is used to print out the current column so that you can monitor the progress of the macro. It is important to note that output to the text window is rather time consuming, and the processing can be sped up by 10-20% if you do not to use it.
If the macro finishes normally or you exit the macro early, then control transfers to this section. A cmx command is given to close the open matrix. Control is returned to the menu interface.
The supplied precoded processing macros (in the Macro pulldown) provide an alternative to writing your own processing macros. These macros are designed to process the most common kinds of 2D data. These macros do not provide the same flexibility inherent in writing your own custom macros, but they do offer the capability to quickly process 2D data collected with most of the typical acquisition schemes.
The precoded 2D processing macros are accessed with the Macro/2D Data Processing menu item. A file-selection control panel appears, from which you can select the data type: FELIX old and new data (.dat) file, FELIX matrix file (.mat), Bruker fid or ser file, Varian fid file or JEOL Alpha or Lambda file, and the filename. If FELIX can access the data, then it opens a second control panel with the header parameters - the acquisition parameters can be valid only if the appropriate files are present (for Varian the procpar file and for Bruker the acqus and the acqu2s file. For Bruker the program also attempts to read the pdata/1/procs and proc2s files.) In this control panel, you can update the header parameters if they show incorrect values.
When you select D1 dimension for processing you are presented with a menu of choices which define how the D1 dimension is to be processed. For more information on each of the various processing options see Chapter 4, Processing, visualization, and analysis interface (1D/2D/ND). When you select OK, the macro first builds a real matrix of the size that you specified with the Dimension 1 Size and Dimension 2 Size parameters. The macro then reads in each of FIDs from the specified input file, processes the data according to the options you selected, and saves the processed vector to the matrix. The macro completes when each of the FIDs, as specified by the D2 Parameters Data Size header parameter, has been processed.
When the D1 macro has finished you will have a FELIX matrix file (normally with a .mat extension) with each of the D1(t2) vectors processed. At this point you can process the D2(t1) vectors by again selecting the Macro/2D Data Processing menu item and choosing the matrix from the previous processing. Then you are again presented with a menu of choices, which in this case defines how the D2 dimension will be processed. When you select OK to begin processing the D2 dimension, the macro opens the matrix you have selected, reads each of the D2 vectors into the workspace, processes each vector according to the options you selected, saves the processed vector back to the matrix, and closes the matrix. When the D2 processing macro completes you will have a FELIX matrix file where all of the D1 and D2 vectors have been processed.
As part of the transformation process it is a good idea to check the data and verify that everything is correct at each stage before proceeding to the next stage in the transformation process. The first check is to make sure that the raw data are correct or that the spectrometer-format data was correctly converted to a FELIX old- or new-format data file. To do this you can use the File/Open menu item to examine the individual FIDs that make up the input data file. By changing the Dimension parameter between 1D and ND, you can control whether this action always reads in the first FID in the series or that subsequent reads load in successive FIDs from the input data file. Once you have verified that the input data file is correct, it is a good idea to experiment with processing the first FID in the series to determine the optimum processing parameters for the D1(t2) dimension. Only after you have determined a good set of starting parameters to use for the D1 dimension should you proceed to processing the entire D1 dimension using a matrix.
Whether you choose to process your data using the precoded processing macros or your own custom macros, the process of transforming your data in the D1 dimension is basically the same. The macro generally first builds a new real matrix to hold the data, reads in each FID from the input data file into the workspace, processes each FID in turn, and stores the result to the matrix. At this point in the processing, you will have a FELIX matrix file where all the D1 vectors have been processed but none of the D2 vectors have been processed. You need to examine the matrix at this point to make sure that the D1 processing is acceptable. It is a good idea to open the matrix file, extract 1D slices (using the View/Draw 1D Slices menu item), and then examine the individual 1D vectors using menu items such as View/Limits/Manual Limits. The View/Draw 1D Slices menu item is especially helpful because it allows you, through the use of a slider, to scan through the individual D1 vectors in order, to determine if the data needs to be reprocessed. If you decide that the basic processing operations such as apodization and solvent suppression were performed correctly, then you generally do not have to fully reprocess the D1 dimension. It is possible to rephase or baseline flatten the existing data. To rephase the D1 dimension you could use the Macro/Phase menu item. To baseline flatten a matrix that has already been transformed in the D1 dimension, you could use one of the Macro/Baseline menu items. You can of course write your own macro to rephase or baseline correct the data in the D1 dimension. Once you have determined that the D1 dimension has been processed correctly and have reprocessed the data if necessary, it is then a good idea to look at some of the D2 vectors. Select some peaks in the first transformed row that you expect to have strong cross peaks and note the point numbers. Alternatively, you could use the Vertical 1D Slice icon to select an initial column vector to view, then use the left and right arrows on the keyboard to scan through a series of column vectors noting the D1 point numbers for a few columns which show a strong interferogram. It is often desirable to load these selected columns into the workspace using the View/Limits/Manual Limits menu item and then save them to FELIX data files. Use these saved column vectors to determine the optimum processing parameters for the D2 dimension. Once you have decided on the optimum processing parameters for the D2 dimension, you can move on to processing all the D2 vectors using your own macros or the precoded processing macros.
Whether you process the D2 dimension with your own macros or the precoded macros, the basic process is the same. The macro opens the appropriate matrix, reads each column vector into the workspace one by one, processes the vector, saves the vector back to the matrix, and closes the matrix file. After you have transformed the D2 dimension, you need to examine the individual D2 vectors using either the View/Limits/Manual Limits or the Vertical 1D Slice icon. If the D2 vectors need to be rephased or baseline corrected, you can do this with your own macros or the precoded macros in the Macro pulldown as discussed above for the D1 dimension.
Throughout this documentation, we use the terms R1 and R2 for the relaxation rates, which are simply the inverse of the relaxation times T1 and T2.
We assume that R1 and R2 relaxation data and heteronuclear NOE were measured as a series of 2D HSQC (or equivalent) spectra (Skelton et al. 1993). You have to pick peaks in one of the relaxation spectra or in an equivalent HSQC. Peak assignments are helpful, but not necessary.
The first step in relaxation analysis is to evaluate peak heights or peak volumes in a series of 2D spectra using the Measure/Relaxation/Measure Heights/Volumes menu item. In practice, peak heights have proved more reliable and yield better signal to noise ratios (Skelton et al. 1993). FELIX automatically centers the peak boxes (if they were picked in another spectrum and are slightly off) and then determines the peak heights or volumes in the relaxation spectra.
For peak-volume determination, the raw volumes are optimized by fitting a 2D Gaussian function to the spectra and deriving volumes from the fit. In the first spectrum of the series, peak widths are optimized, then peak amplitudes, and finally both are optimized simultaneously. In subsequent spectra, centers and widths are left as they are, and only amplitudes are adjusted. For peak-height determination when peak boxes overlap, the peak box is iteratively shrunk by one point in each dimension until no other peak box overlaps it, to prevent cross talk from any overlapping peak maxima.
Thus volumes and heights are accurate within the limits of the methodology even for overlapped peaks, and the procedure requires no interaction on your part. Peak heights or volumes are stored into a regular FELIX volume table, but the last row holds relaxation delays instead of mixing times.
The next step is to estimate the signal-to-noise ratio from one or more duplicate spectra, using the Measure/Relaxation/Signal/Noise Ratio menu item. The average standard deviations obtained for these spectra are interpolated to the other points in the series as appropriate. The time courses of peak heights/volumes that you obtain in this way can be visualized and plotted by:
1. Selecting the Measure/Relaxation/View Timecourse via Cursor menu item and then selecting a peak with the mouse.
2. Selecting the Measure/Relaxation/View Timecourse via Item menu item and entering a peak number.
If the time series is already fitted to an appropriate exponential function, this function is also displayed, and the relaxation rate is reported in the text window.
Duplicate peak volumes and heights are stored in their own volume table, which is essentially a copy of the original volume table, with the appropriate column overwritten with values from the duplicate spectrum. Uncertainties are found in the last row of this table.
After obtaining peak heights and volumes and their errors, you can fit these time series to an appropriate exponential function (using the Measure/Relaxation/Fit R1/R2/NOE menu item). For R1 data, this is a general exponential function:
where R1 = -a2.
For R2 data, where in theory the values decay to zero, the simpler equation:
where R2 = -a1 may be appropriate. In practice, it is often found that the more general Eq. 37 yields statistically better fits (Skelton et al. 1993). FELIX tries both fits and retains the coefficients for the fit with the lower c2 value.
Heteronuclear NOE data are analyzed in a single step using the Measure/Relaxation/Fit R1/R2/NOE menu item. After obtaining the filenames for the spectra obtained with and without 1H saturation, FELIX again centers the peak boxes (see above) and then proceeds to determine peak heights or volumes as desired. Next, two duplicate spectra are analyzed to derive the uncertainty of the measurement. The NOE is the ratio of the volumes obtained with and without 1H saturation.
In addition to generating R1, R2, and NOE values, the relaxation analysis tools provided in FELIX let you prepare input data files for the Modelfree program of A. G. Palmer (accessed via the Measure/Relaxation/Modelfree Input menu item). Modelfree can be downloaded from Columbia University's website at
For further details on analyzing relaxation data with the Modelfree program, see Mandel et al. (1993).
The assignment work starts with defining a project. It is highly advisable to define only one project within one database file. The project then contains all the information needed in the course of the work, such as spectrum definitions, last display parameters, and entities necessary to store the assignment information.
The definition of the project starts with reading in an Insight II or X-PLOR coordinate file of the molecule (or complex) being studied. This coordinate file does not necessarily need to be the true structure, especially since at the beginning of the assignment the final structure is not usually known. As the assignment progresses and refined structures become available, the new coordinates can be read into the project.
The crucial part of residue identification is the library. The library is an ASCII file, where the mean chemical shifts and standard deviations are listed for the usual residues. You can change these values and can also add non-standard residues to the end of the file. This procedure is illustrated later. This file is then read into the project and used in spin-system identification.
You can define the matrices that are used in the assignment. These matrices should be referenced in ppm and are in the standard FELIX format. In adding the experiments, it is important to define a reasonable tolerance for each axis, since the automated spin-system detection routines rely heavily on them. This tolerance should mirror the uncertainty of the peak positions in each dimension (in ppm). Later on you can delete unused experiments from the database and add new ones. For example, you can start with J spectra (TOCSY, DQF-COSY, HSQC-TOCSY, or CBCA(CO)NH) to do the sequence-specific resonance assignment. Once that is done, you can delete the J spectra and define NOE-type experiments (e.g., NOESY or HSQC-NOESY) to do peak assignment and restraint generation.
If you work with non-standard amino acids or nucleic acids, you can add these new residue types to the database, by simply editing two files in $BIOSYM/data/felix/asglib/ with any text editor. One file contains the residue definition (atoms, median chemical shifts, standard deviation, and topology), and the other contains the alias names.
The residue-definition file is called pd.rdb or rna.rdb. For example, to add an aminobutyric acid residue, you should go to the end of the pd.rdb file, which looks like:
! ROOM FOR MORE RESIDUE TYPES ...
1. Each line that starts with an exclamation mark is a comment. So first you add the formula as a comment:
! ABU (aminobutyric acid)
! H - N H
! | |
! H - Ca - Cb - Cg - H3
! | |
! O = C H
2. The next part of the file is the residue name:
RESIDU ABU X
where X is just a one-letter shortcut for the residue name.
3. Now you need to enter the atoms:
First enter the keyword RESATM, then the atom type, atom name (in Insight notation), a number (this field is not active yet), a mean chemical shift, a standard deviation, and finally, if there is more than one atom (e.g., a pseudoatom) in that group, enter the number of atoms.
This section of the file should now look something like:
RESATM H HN 1 8.16 0.60
RESATM H HA 2 4.30 0.20
RESATM H HB1 3 3.30 0.20
RESATM H HB2 3 3.30 0.20
RESATM H HG* 4 1.10 0.10 3
RESATM N N 8 126.0 5.0
RESATM C CA 10 51.0 5.0
RESATM C C 9 150.0 50.0
RESATM O O 15 0.0 999.0
RESATM C CB 12 26.0 5.0
RESATM C CG 12 17.0 5.0
4. Next is another comment line that contains the atoms used to help construct the neighbor matrix:
! HN HA HB1 HB2 HG* N CA C O CB CG
5. The next part of the file is the connectivity matrix:
Each element shows how many bonds are between the constituent atoms (groups).
CONECT 3 0
CONECT 4 3 0
CONECT 4 3 2 0
CONECT 5 4 3 3 0
CONECT 1 2 3 3 4 0
CONECT 2 1 2 2 3 1 0
CONECT 3 2 3 3 4 2 1 0
CONECT 4 3 4 4 5 3 2 1 0
CONECT 3 2 1 1 2 2 1 2 3 0
CONECT 4 3 2 2 1 3 2 3 4 1 0
6. Finally a keyword finishes the residue definition:
The other file to edit is the .alias file.
7. Append a line to the alias file which contains the names of that residue for all the charged/terminal forms:
ABU ABUN ABUC ABUn
After these two files are edited, Assign can deal with the new residue type.
Usually the first step in assignment is peak picking. FELIX has two types of peak pickers: the regular one and one that uses example peaks to distinguish genuine peaks. Depending on the data, it is probably advisable to try several rounds of peak picking using both methods, and then use whichever filtering functions (such as symmetrizing, deleting the diagonal, and merging multiplets) you prefer. Good peak sets are crucial for the success of the analysis procedure.
After picking peaks, you may want to use peak optimization to better define the peak centers, widths, and/or volumes. To do this you need to first measure the peak volumes. Sometimes the peak optimizer can merge close peaks; therefore, it is advisable to measure the peak volumes interactively and save the peak entity in a backup file within the database. By defining small regions where the optimizer should work and examining the results, you can see if the peaks get misplaced too much or merged unnecessarily. Then you can retrieve the saved copy and omit optimization for those peaks.
In assignment work you often need to analyze multiple spectra simultaneously. To help with this, FELIX allows you to connect multiple frames so that the definition of plot limits in one frame automatically triggers the same changes in the other connected frames.
To connect frames, use the Preference/Frame Connection menu item. To illustrate the process, let's assume you have a CBCANH and a CBCA(CO)NH experiment. The CBCANH was transformed so that D1 is 13C, D2 is 15N, and D3 is 1H. Let's assume that CBCA(CO)NH was transformed so that D1 is 1H, D2 is 13C, and D3 is 15N. Let's also assume that you want to see 1H-13C slices, and that CBCANH is the experiment in Frame 1 and CBCA(CO)NH in Frame 2. In Frame 1 you would select the CBCANH spectrum from the Experiment table and in Frame 2 you would select the CBCA(CO)NH spectrum. After going back to Frame 1 and selecting the Preference/Frame Connection menu item you would do the following:
1. In the control panel, leave the First Frame set to 1 and the Second Frame as 2.
2. For the connection method, choose the D1-D2-D3<=>D1-D2-D3 radio button and then select OK.
Now, if you zoom in on a region in the CBCANH spectrum (Frame 1), then the same plot limits are defined in the CBCA(CO)NH spectrum (Frame 2). Similarly, if you step onto another plane (for example, in the CBCA(CO)NH spectrum (Frame 2)), then a plane at the same 15N frequency is displayed in the CBCANH spectrum (Frame 1).
Certainly, if you have 2D, 3D, and 4D spectra to connect, you can use this interface to define quite sophisticated schemes. The following is a theoretical example of how you would connect a 2D spectrum with 3D spectra:
1. Assume you have a 2D 15N-1H HSQC spectrum with 15N as D2 and 1H as D1. Let's moreover assume that you have a 15N TOCSY and 15N NOE spectra, where D1 is the amide 1H, D2 the full 1H, and D3 the 15N dimension. You want to look through the amide peaks in the HSQC spectrum and then see the corresponding slices in the TOCSY and NOESY spectra. First you would select the HSQC spectrum from the Experiment table for Frame 1 and the TOCSY and the NOE spectra, respectively, for Frame 2 and Frame 3.
2. In the first control panel leave First Frame set to 1 and Second Frame set to 2. This connects the HSQC spectrum with the TOCSY spectrum. Select the Custom option and select OK. In the next control panel, set:
3. Toggle Define Jump to on and for Jump Direction set:
4. Select OK.
5. Next, connect the HSQC spectrum with the NOE spectrum with the first control panel (which should appear again). Leave the First Frame set to 1 and the Second Frame to 2. Select the Custom option and select OK. In the next control panel, set:
6. Toggle Define Jump to on and for Jump Direction set:
7. Select OK.
8. Linking all these spectra assures that plot navigation in the HSQC spectrum (e.g., zooming in on a peak) translates to the same movement in the HSQC-TOCSY and HSQC-NOE spectra. If you press the period <.> on the keyboard while in the HSQC frame you will be able to use the cursor to select a new 15N position (e.g., clicking on a HSQC peak), which then translates to new planes also in the TOCSY and NOE spectra.
If in addition you want to navigate the TOCSY and NOE spectra together, you need to set that up by using the Preference/Frame Connection menu item again.
9. Make Frame 2 current. Select the Preference/Frame Connection menu item. In the first control panel, leave First Frame and Second Frame set to 2 and 3, respectively. Select D1-D2-D3<=>D1-D2-D3 as the method and select OK. After the control panel appears again, select Cancel. This way you have connected all three axes of the TOCSY and NOE spectra.
The key step in sequential assignment is spin-system detection. In FELIX spin systems are detected in three stages:
1. The first type of spin system results from automated spin-system detection. These are called prototype patterns or protos. This system can be intraresidue or can contain spins from neighboring residues, depending on the spectrum and method by which the data were collected.
2. The second type of spin system is the frequency clipboard, which is a unique list of frequencies that originates from a proto or a concatenation of several protos, or which are hand picked from a spectrum. The clipboard is usually where you would delete spurious resonances from the spin system or add missed resonances manually.
3. The third stage of spin-system detection is the so-called pattern. Patterns can be scored against a library to find a type probability score or they can have sequential neighbors. The frequencies in the pattern may also then be assigned to atoms (or atom groups) in the molecule. Patterns can be edited, but with much more limited functionality.
At each stage, the spin system can be visualized by spawning tile plots or strip plots or by drawing lines along the frequencies. Visual interaction is an important element in assignment, since automated routines are not 100% reliable.
You can collect spin systems manually, that is, by picking peaks in a spectrum and promoting the chemical shifts to the clipboard. You would typically do this if there were unresolved or missed spin systems left after automated spin-system detection. Then you would go through the spectrum (or spectra) and use the controls in Assign/Frequency Clipboard to collect the peak positions as frequencies in the clipboard. After each spin system is collected this way, you then need to copy it to patterns and clear and start over with the next spin system.
The automated prototype pattern-detection routines work on one or several peak-picked spectra, depending on the method selected. You should optimize the values of several parameters by trial-and-error. To find as complete a set of spin systems as possible, several iterations are necessary. Guidelines for selecting prototype pattern parameters are given below.
One of the most important variables in automated spin-system detection and neighbor-finding methods is the tolerance. A spectrum-specific tolerance for each experiment needs to be entered at the beginning. This number usually represents how well the peaks are lined up in each dimension up for any given frequency, that is, how much the peak centers differ along a particular dimension arising from the same spin system. As a rule of thumb, this number is roughly equivalent to the digital resolution in ppm (e.g., first try the ppm equivalent of one point, which then will use this number as a boundary - each peak whose center is within the target plus/minus the tolerance). This tolerance is used to automatically assign peaks to frequencies.
Another tolerance is also required during automated spin-system detection, which is sometimes needed to decide whether a peak belongs to a spin system. If you use the homonuclear method with one spectrum, this tolerance is defined by the resolution of the dimension having the worse digital resolution in ppm, usually the F1. If you use multiple spectra, then this tolerance should be defined based on a comparison of the chemical shifts of the peaks belonging to the same connectivity in different spectra.For example, if you measure the position of a couple of the "same" peaks in the NOESY and TOCSY spectra, the difference defines the tolerance. Certainly, if the automated methods do not give sufficient results, the first thing you should try changing is the tolerance.
It may of benefit to reference one base spectrum and also newly introduced chemical shift ranges in other spectra, according to scientific theory, and reference the other spectra so that known peaks match optimally. This can significantly increase the success of automated spin-system detection and peak-assignment routines.
The 2D systematic search method can be used on different combinations of COSY, TOCSY, and NOESY type spectra. In the first iteration for a protein, the spin systems are usually collected starting from a Ha-HN cross peak, then the full spectrum is searched for aligned peaks that define new frequencies. Therefore, the seed region should be set to an Ha-HN region either above the diagonal or below, depending mainly on resolution and on the presence of possibly spurious peaks. The frequency collapse tolerance then defines whether the new frequencies (possibly resulting from different spectra) are unique. It is useful to try several settings for this number, but you can start by guessing how well the corresponding peaks in different spectra are aligned.
These settings must be changed if, for example, you want to find the possible prolines: the seed region should then be at the Ha-Hb region, and you must exclude spin systems having frequencies in the aromatic/amide region. Similarly, if you want to search for aromatic side chains, you must use the aromatic region as a seed and exclude the aliphatic region by filtering.
Between iterations, you can selectively delete prototype patterns that are clearly not right, thus releasing peaks, or you can delete all of them. Also, it is useful to note that after you assign or define several reliable patterns, then those patterns' frequencies can be copied back to prototype patterns, thus preventing you from re-detecting them in the following iterations.
This search should begin with the longest spin systems. Since the algorithm tries to fit peaks into a defined motif, it does not take care of possible additional correlated frequencies, which means that an AMX portion of a long spin system could be assigned to a four-spin system. Initially, the program should be run on the whole residue set of the primary sequence (which automatically takes the above priorities into account) and on the patterns examined with the usual interactive tools. Then it should be rerun on specific missing amino-acid types. To compensate for the limited number of iterations in simulated annealing, the process should be run for several loops (typically 6), from among which the program will retain the best results. One loop of the program for the whole sequence of a 53-residue protein requires about 10 min of computation time on an R4000 Silicon Graphics Indigo workstation. For aromatic residues, this method assigns only the AMX subsystems; therefore, the aromatic resonances should be found with the systematic search method and added through the clipboard.
Double-resonance spin-system detection is implemented in two different ways: one method which finds spin systems starting from the backbone, and one which finds spins in existing spin systems and extends them.
The first method works on 15N-1H HSQC-TOCSY and 15N-1H HMQC-TOCSY spectra. For this method, the spectrum should contain pseudodiagonal peaks - that is, HN-HN-N peaks - from which the spin systems will be collected along the sidechain. If the pseudodiagonal is not well resolved or if peaks are missing, you can use the 15N-1H HSQC spectrum to help - the program tries to find new frequencies in the 3D from each peak in the 2D spectrum and stores them as spin systems. However, if the 15N-1H HSQC spectrum is not well resolved, this method is less effective.
In the second spin-system detection method, you can use double resonance experiments to extend already existing spin systems - usually these are results of a triple-resonance spin-system detection run. Here, the purpose of the detection is to expand spin systems containing only backbone frequencies, to include sidechain information. Currently one method is implemented in FELIX which uses a 3D HCCH-TOCSY spectrum to achieve this. You can expand spin systems in the prototype pattern stage or in the pattern stage.
A variety of triple resonance measurements can be used for making sequence-specific assignments. Several approaches are implemented, which have some common elements: usually you must first peak-pick several triple-resonance spectra and find out what the uncertainty is between the peak positions within each spectrum for a couple of resonances. This will be the spectrum-specific tolerance for each axis. Also, you need to find out, simultaneously inspecting the spectra, how well the peaks belonging to the same resonances can be overlaid. For example, you need to know, at a given X residue, what are the differences between the peak frequencies along the HN and 15N axis, and Ca in the HNCO and HNCA and HN(CO)CA spectra (HN,x-Nx-Cx-1, HN,x-Nx-Ca,x-1, and HN,x-Nx-Ca,x-1, respectively). Those will be the interspectrum tolerances for the respective axis.
After that you can run one of the spin-system detection routines starting with, for example, a tolerance that is a little less than these inter-spectrum tolerances, and then telling the program to iterate and increase the tolerance at each iteration step. Depending on the spectrum quality, you can automatically get 50-90% of the theoretical spin systems. These spin systems may not be perfect; therefore, you need to inspect them before promotion and discard or alter any inadequate spin systems. Also, you can manually add missed spin systems to the list of prototype patterns. There is an advantage, since usually triple resonance experiments are measured as (at least) pairs, so if you add spin systems at this stage, you can manually add frequencies belonging to this residue as well as to the neighboring residue. As long as you let the program know what those frequencies are, then Assign will establish these connectivities in the promotion stage.
In addition to the predefined combinations of experiments given here, you can design your own spin-system detection methods. Typically you would design your own protocol if you have a good-sensitivity 2D or 3D double- or triple-resonance spectrum (e.g., 15N HSQC or HNCO), known as a "seed" spectrum, together with a couple of double- or triple-resonance 3D "secondary" spectra (e.g., HNCA and HN(CO)CA). The typical procedure is to start from the seed spectrum with each peak as a trial peak and try to collect connected resonances in the secondary spectra. For example, if you want to detect spin systems using a combination of HNCA and HN(CO)CA experiments, you can use the following procedure (assuming that the order of dimensions is HN, N, Ca):
1. First, select the Assign/Collect Prototype Patterns/User Settable menu item and set the Number of steps to 1, since the seed peak selection is considered as the zeroth step. Select the HN(CO)CA spectrum as the seed spectrum (Step # 0) and the HNCA spectrum as the first step.
2. Since you need to match the HN and N frequencies in the two spectra for the corresponding peaks in the second control panel (Experiment hncoca in Step 0), you select the following for the Match to parameters:
3. For the D1 Type select HN, for D2 Type select N, and for D3 Type select null. The typical tolerances would be comparable to the differences between the chemical shifts of the same HN-N-Ca peak in the two spectra, for example, 0.02, 0.15, and 0.15 ppm for D1 Tol, D2 Tol, and D3 Tol, respectively. You can perform selective detection using chemical shift ranges to reflect that, or you can use the full spectrum using -1 for all Range variables. Typically, several trials are needed from each peak, to find a prototype pattern.
The next set of variables reflects this, that is, if with the given tolerances not enough frequencies (Minimum Freqs in Proto) are collected from a particular peak, then new iterations are carried out (up to Number of Iterations times) increasing the tolerances by the Tolerance Factor. You can also direct the program to delete peaks that may belong to already detected spin systems (Remove First is then True). For this, you would select 3 for the Number of Iterations and 1.2 for the factor by which the tolerances are multiplied after each unsuccessful trial (you need 4 frequencies).
4. In the next control panel you must decide how many peaks to store and which frequencies to store. Here, we need to use the D3 frequency (the 13C dimension) (Use D3) and you need to store the frequencies for two peaks (Store 2). The Type variable is active if you select the All option for Store (it is useful in, e.g., a 15N-HSQC-TOCSY experiment, because the program would not assign the resonances along the TOCSY line but would call them HXs). You set the first peak's frequency to store as Ca (this peak in the HNCA spectrum is usually more intense: #1 CA and Attr Larger). The second peak's D3 frequency then results in the Ca,i-1 frequency (#2 CA(-1) and Attr Smaller). Besides the magnitude of the intensity, you can use the sign of the intensity as a distinction (as for the HNCACB spectrum, where the HN-N-Ca and HN-N-Cb peaks have opposite signs) or use a distinctive chemical shift range.
This procedure makes it possible to collect spin systems automatically in the user-defined combination of spectra.
You can collect spin systems using a semiautomated method. Here, you use the cursor to select a peak in one spectrum, and the program then tries to extend this trial spin system in the spectra that you connected to it. To illustrate: let's assume you have a 2D 15N-1H HSQC spectrum with 15N as D2 and 1H as D1. Let's moreover assume that you have a 15N TOCSY, where D1 is the amide 1H, D2 the full 1H, and D3 the 15N dimension. You want to select an amide peak in the HSQC spectrum and then let the program collect frequencies in the corresponding slice of the 15N TOCSY spectrum.
1. First you select the Assign/Collect Prototype Patterns/Semiautomated Setup menu item and set the Number of frames/steps to 2, putting the HSQC in Frame 1 and the HSQC-TOCSY in Frame 2.
2. In the second control panel, select the following for the Connect to parameters:
3. Now set the Slice Position in Frame 1 parameter to D2 and the Sliceplane in #2 to Along D3. That means that you want to use the D2 coordinate of the HSQC spectrum to select a plane in HSQC-TOCSY along D3.
4. Next you must specify how to match the different frequencies. Here, you need to match the D1 of the HSQC to the D1 of the TOCSY, and the D2 of the HSQC to the D3 of the TOCSY spectrum (HN to HN and 15N to 15N). You also need to specify the spin types you expect in this first spectrum, together with search tolerances: HN with 0.02 and N with 0.1.
5. The number of iterations can be set with a tolerance factor, which specifies that the spin-system collection is be tried that many times, increasing the tolerances that many times (you can set it to 3 and 1.4, for example).
6. In the third control panel you would set the Orientation parameter D1-D2 to D3: 118 ppm. You would set the Connect to parameters as follows:
7. Now set the Use parameter to D2 since you want to collect new frequencies along D2 of the HSQC-TOCSY spectrum (with D1 and D3 defined by the HSQC) and Store All with type HX.
This setup then would make it possible to zoom in on a peak in HSQC and on a strip in HSQC-TOCSY. Moreover, if you want the 15N position from HSQC transferred to 3D spectra, you need to press the < . > key to activate the hidden Jump function. This function gives you a cursor: clicking the required peak (or 15N position) with this cursor triggers a jump to a new slice. Finally, if you find a peak in the HSQC spectrum where you want a new spin system to be collected, you need to select the Assign/Collect Prototype Patterns/Semiautomated Collect menu item (for which the hotkey is =) and click that peak with the crosshair cursor. If the program can find connected peaks in the HSQC-TOCSY spectrum, it collects the spin system and shows it in the prototype pattern table.
Most of the automated methods in the Assign module collect spin systems containing backbone atoms. To automatically extend the spin systems to include atoms from the sidechain, you may want to run the routines accessed from the Assign/Collect Prototype Patterns/Extend Prototype Patterns menu item. To illustrate this method, let's assume that the spin systems were collected so that the prototype patterns contain the HN, N, Ca, and Cb shifts. Then you can use a 3D HCCH-TOCSY spectrum to automatically find the corresponding Ha, Hb frequencies. In the Extend Prototype Pattern Using HCCH-TOCSY control panel, you would select appropriate tolerances for the search along the 13C and 1H dimensions (taking into account how well the Ca and Cb resonances align between the spectra they were detected from (e.g., CBCANH) and this spectrum). You have to set how many times the extension will be attempted from each prototype pattern (Number of iterations) and how much to increase the tolerances each time (Tolerance factor). You also have to define the primary and secondary search dimensions for protons, as well as the carbon dimension. The primary proton dimension is where the heteronuclear transfer was done, and the secondary dimension is where the TOCSY was done.
You can use the extend option to add Ha,i-1 and Hb,i-1 frequencies to spin systems containing HN and N frequencies using the HBHA(CO)NH spectrum (Extend Prototype Pattern Along One Axis).
As soon as reliable spin systems are detected, you can promote them to patterns. This can be done in two ways.
One way is to copy the protos one by one, using the clipboard. This is the preferred method for spin systems detected in homonuclear or heteronuclear double-resonance spectra, since it is wise to visually inspect and correct the results of automated methods. After inspecting and correcting the frequency clipboard you can verify that the new "pattern" is unique by using the fuzzy algebra comparison control panel (Assign/Frequency Clipboard/Compare Frequencies menu item).
The other way, which might be more dangerous if you did not verify the prototype patterns, is to copy all prototype patterns to patterns directly. If you choose this method, you must delete false prototype patterns before copying. This method is preferred for prototype patterns resulting from triple-resonance heteronuclear spectra, since the neighbor information contained in protos detected in triple resonance spectra can be preserved this way.
The next step in peak assignment is to identify the spin systems - the patterns resulting from an automated or manual search. This can be done in Assign based on all-atom chemical shifts contained in the database, by using either a simple scoring algorithm or by using a probability distribution for Ca/Cb chemical shifts (Grzesiek and Bax 1993). The latter method gives better scores, since the proton chemical shifts are not so well dispersed for different residue types, but this method can only be used if labeled proteins are accessible.
The all-atom method gives scores that are not very distinguishable from each other, but, combined with the sequential probability scores, it still gives a good starting point for the sequential assignment-generation step. To help with the assignment, it is advisable to manually unset scores based on a DQF spectrum of the very unlikely residue type probabilities.
This is the next step in the sequential assignment strategy. Usually this step uses the NOE effect as its basis, but in triple-resonance spectra, this connectivity shows up in J peaks, therefore the J-peak-based method is more reliable. Nevertheless, because of the difficulties encountered during labelling, and because a significant portion of the connectivities do not show up due to spectroscopic reasons, the NOE-based methods are still important. The Assign module includes several menu items that deal with the sequential connection of patterns. It is advisable to have a possibly full set of patterns when you start to find sequential connectivities. Also, it is important that the spectrum-specific shifts be set correctly for the NOE spectrum that is to be used to find the sequentials. The root frequency for each pattern also should reflect the real (average) HN frequencies of the NOE spectrum for the homonuclear neighbor-finding methods.
You can use the Assign/Neighbor/Find Neighbor Via 2D NOE or 3D NOE menu item to connect the aromatic sidechains with the aliphatic sidechains. You usually end up with prototype patterns having the aliphatic and aromatic part of the same residue as two different entries. Therefore, you promote them to separate patterns. Then you must find which aliphatic sidechain has several contacts to the Hd's (of Tyrs or Phes) which should be the root frequency for that particular pattern. If you find the correct connection (possibly visually inspecting by tiling) then you must merge the two patterns (you can use the Assign/Frequency Clipboard/Copy Pattern To Clipboard and then the Assign/Frequency Clipboard/Copy Clipboard To Pattern menu items). Lastly, you must delete the purely aromatic sidechain pattern(s).
The Assign/Sequential/Systematic Search menu item can be used to match the sequence on a set of patterns that have at least residue-type probabilities and sequential probabilities assigned. The algorithm is flexible, therefore several strategies can be followed. One approach is to generate all possible assignments for the entire molecule (Min length of assigned stretches = full sequence). Here, the assumption is that the best scores will result from the correct assignment, but the Min neighbor prob score variable should be set to 0, since there can be missing sequentials. This could mean that the number of possible assignments will be very large (Kleywegt et al 1993),but restricting the Max # of assignments to generate variable to a small number (100-1000) can give a usable result.
The other approach would be to assign shorter stretches (20-30 residues), still keeping the neighbor probability score comparatively small (e.g., 0.1). This method has the disadvantage that you cannot assume that the first solution is the correct one; therefore, you must check all high-scoring possibilities.
The third approach was named "iterative assignment by consensus" (Kleywegt et al 1993), which means that assignment generation starts with restricting the neighbor probability score to high values and letting the Min length of assigned stretches be relatively small. Thus, well connected stretches are found first, then the neighbor score is gradually relaxed and the minimum length is increased, and longer, well defined stretches are assigned. This procedure continues while no new assignments can be obtained. Then you might try to specifically assign the remaining stretches. At all stages the consensus means that those residues are assigned which are conserved in a majority of generated assignments.
The Assign/Sequential/Simulated Annealing menu item can be used on any set of homonuclear or heteronuclear patterns. It uses only the type and neighbors scores, obtained by any method, to find the sequence-specific assignment. Optionally, previous assignments are loaded and respected. The amino acid type and/or residue number are considered assigned for a pattern, if they are consistent over all frequencies of the pattern (unique or specified assignments).
After careful inspection of the patterns and scoring of types and neighbors, the process might be run on the full sequence. Then you might inspect the result, modify it using the Pattern Assign functions, perhaps try another run, and identify some satisfactory parts from the scores listed. You should then discard the ambiguous assignments and rerun the program with the correct residues used as anchor points. If several such iterative processes fail to unambiguously determine the complete assignment, then some additional information should be input, such as more accurate scoring or some new patterns.
The results are stored as assignment pointers for all frequencies of the patterns (and set as the current specified frequencies). There should not be any residue named "null" in the molecule, or its assignment will be discarded.
Optionally, some parameters of the simulated annealing might be adjusted (scaled by a factor of 0.1 to 10) according to the complexity of the problem:
When you assign particular resonances or frequencies in the patterns, you need to use the Insight II atom names if you plan to use NMR_Refine to generate or refine structures. If you make the assignments through the control panels, the atom names are automatically correct. The usual form of the so-called nmrspec is: 1:RESIDUENAME_RESIDUENUMBER:ATOMNAME(NUMBER) (e.g., 1:VAL_4:HN). If you need to use pseudoatoms, then the specification is: 1:RESIDUENAME_RESIDUENUMBER:ATOMNAME(NUMBER)*.
For example, one of the methyl groups in valine would be named 1:VAL_4:HG1*, which encompasses atoms 1:VAL_4:HG11, 1:VAL_4:HG12, and 1:VAL_4:HG13. The methyl group in alanine would be named 1_ALA_23:HB*, which encompasses methyl protons 1:ALA_23:HB1, 1:ALA_23:HB2, and 1:ALA_23:HB3.
After the resonance assignment is finished, you can try to assign your peaks (usually in an NOE spectrum). It is very important to have spectrum-specific shifts for all patterns that are as good as possible, since otherwise peak assignment can be very ambiguous. You can adjust the spectrum-specific shifts manually or automatically. Preferably you would do it both ways: first automatically, then manually for what was missed. After this is done you can make auto-assignments.
You can approach the automated assignment in different ways: you can use a linear chain as a model and only assign intraresidue and sequence peaks, as well as peaks having unique frequency assignments (that is, peaks that have only one possible assignment in each dimension), or you can use a homology or a low-resolution starting model (for example, from x-ray crystallography) and assign based on those distances. Or you can make ambiguous assignments and then later use those assignments as overlap restraints in SA or rMD protocols.
After a set of assignments is generated and (possibly manually) verified, structures are generated based on them. You can refine your assignments based on the new model or based on hotspots (where restraints are highly violated or the structure is bad).
A crucial step in generating NOE distance restraints is to define suitable scalar peaks, that is, those peaks for which the assigned atoms are in a rigid part of the molecule and which are associated with well defined distances. These peaks are often referred to as "reference peaks" and are used to calibrate the conversion of peak intensities (volumes) to distances. As a rule of thumb, it is always safe to use good-intensity, clean, non-overlapped peaks as scalars. One category would be HB1 to HB2 methylene peaks in the same residue. You can also use an intraresidue HN-HA peak as a scalar, since the variability of this distance is small across different secondary structures. If you use either single mixing time (Single tm) volumes or volume buildups through fitting (Fit First N tm) for calculation of the restraints (Calculation Method), you need to have scalar peaks for which the distance is roughly equal (e.g., use only methylenes or only intraresidue HN-HA peaks). On the other hand, if you use an empirical fit of volumes versus distances (Calculation Method is Empirical Fit), then you typically need several types of peaks - representing some short, some medium, and some longer distances. FELIX then fits an empirical function through the volume/distance pairs, and the volume is converted using this empirical fit.
If you use a 2D NOESY spectrum, you may want to control which peaks' volumes (Symmetry Selection) are converted to distance restraints. Use All converts all peaks (and then only restraints are generated for the first occurrence of the symmetric pair), Select Regions uses different sides of the diagonal in certain regions of the spectrum, and Use Weaker uses only the weaker peak of a symmetry-related pair.
Converting the calculated distance to a restraint can happen in many different ways (Method): Exact Distance, S-M-W Bins, VdW-Exact, Percentage. The most dangerous method is using the exact distance as a restraint (Exact Distance) - in this case the lower and upper bounds become that calculated distance. The most popular method is to carry out a categorization into the strong, medium, and weak categories (S-M-W Bins) and to store the corresponding bounds in the restraint. The third method is to set the lower bound to the van der Waals distance and the upper bound to the calculated distance (VdW-Exact). In the fourth method (Percentage), you specify a percentage by which the calculated distance will be decreased and increased to yield the lower and upper bounds.
There is always a danger in doing a totally automated conversion - there can be overlapped peaks where the measured volumes do not represent the real volumes. To avoid over-restraining when using such peaks, FELIX can handle this type of peak differently, if you use the Partial Overlap option to check how much the area of integration is overlapped for each peak. You can then define a threshold (Area Threshold) by which the algorithm can skip to generate restraints from those overlapped peaks (Discard) or you can use a different method to generate bounds from calculated distances, (e.g., Use as Qual, which generates only qualitative upper-bound restraints).
After assigning NOE peaks and generating restraints, you would typically run structure calculations either by using distance geometry (the DGII command within Insight II's NMR_Refine module) or simulated annealing (the MD_Schedule command within Insight II's NMR_Refine module). Usually the assignment/restraint generation and structure calculation are done in an iterative way. That means that, after generating a set of structures, you need to analyze the structures and find the so-called hotspots (e.g., where many restraints are violated).
Those hotspots can result from misassignment or overlapped peaks. For misassignment, you use a list to reassign (or unassign) those peaks. You can use a simple ASCII file which just has the two (or three or four, depending on dimensionality) names in a row separated by a blank. You can also create a list within Insight II using this procedure:
1. First load the restraints on all the refined molecules in Insight II using the NMR_Refine modules' Restraints/Read molname* command.
2. Execute the NMR_Refine modules' Distance/List command. On the resulting output file run, the provided numvioltofelix script redirects the output to another file. This is the file you can use in the Filename parameter.
3. Proceed similar to the previously described Manual Assign Singly action, but instead of selecting the peaks with the cursor, the peaks automatically will be centered in your current frame and the corresponding control panel will appear.
Hotspots can also be due to erroneous restraints. If so, the NOE Distance Redefine option in the Measure/DISCOVER Restraints command can help to loosen, tighten, or delete the restraints showing the highest violations (or the most violations within a family). To do this you must:
1. Load the restraints on all the refined molecules in Insight II using the NMR_Refine modules' Restraints/Read <molname*> command.
2. Execute the NMR_Refine modules' Distance/List command. On the resulting output file run, the provided numvioltofelix script redirects the output to another file.
3. Use the Measure/DISCOVER Restraints/NOE Distance Redefine command on this file. You should specify the Restraint entity that you want to work with (usually the msi:noe_dist) and the Buildup Rate Calculation Method. The program brings up a violation table, through which you can zoom in on each peak for which the defined restraint was violated and can report the calculated distance. The table also contains the restrained values and the violation statistics.
4. From the violation table you can redefine the restraints, delete restraints, or delete assignments.
For accuracy assessment of the molecular models or to assist in the assignment procedure, it is very useful to generate back-calculated NOESY spectra to compare with the real NOESY spectrum. To do this, you must have a NOESY spectrum or buildup assigned and know the correlation time of the overall tumbling. In the control panel (from the Model/Matrix Doubling menu item), you also need to enter the spectrometer frequency for protons which was used to generate the experimental spectrum. A reasonable distance cutoff allows the program to calculate only the realistically measurable NOEs, which can be around 7 Å without slowing down the back-calculation too much. Also, since usually not all the NOEs can be measured due to poor sensitivity, you may want to impose a minimum intensity requirement (e.g., 0.005 stands for 0.5% NOE). After the calculation is done (Model/Matrix Doubling menu item) you may want to plot the theoretical spectrum. For this, you must define how theoretical NOEs will be scaled in comparison to the experimental ones. You need to select an assigned peak in the experimental spectrum, for which the intensity will be the same in both spectra.