Legal Stuff
Using BB-Reader
for Scientific Work
Platform
Installing
BB-Reader
What does BB-Reader for you?
Before you
run the program
Getting
started
The output
Groups of
equivalent atoms - ambigous assignment
Calculation
of the score
Nomenclature
of atomtypes
�Logfile
Command-line
arguments
Limitations
(and how to work around)
Feedback
The software and accompanying instructions are provided "as is"
without warranty of any kind. The authors do not warrant, guarantee, or make
any representations regarding the use, or the results of the use of the
software or accompanying instructions in terms of correctness, accuracy, reliabilty, currentness or
otherwise. The entire risk as to the results and performance of the software is
assumed by you. If the software or instructions are defective, you, and not the
authors, assume the entire cost of all necessary servicing, repair or
correction.
BB-Reader is copyrighted software. You may use and distribute it free of
charge, but it must not be sold or offered as an inducement to buy other
products. Moreover modified source-code must not be distributed and the
source-code must not be redistributed without the accompanying files (manual).
If you used BB-Reader for scientific work, and you are publishing that work,
please cite the following article: Wimmer, R., M�ller, N., and Petersen, S.B., "B-B-Reader: A
Computer Program for the Combined Use of the BioMagResBank
and the PDB databases," J. Biomol. NMR 9, 101-104 (1997).
BB-Reader is written in C, and it is designed to run under a UNIX-environment.
It does not have any graphical user-interface.
You can obtain the file BBReader.tar from
http://www.bmrb.wisc.edu/bbreader/BBReader.html
Create a directory and move the tarfile in there.
Extract the files from the archive with "tar -xf
BBReader.tar", and you will find the source-code
("BBReader.c") and the manual as text
("bbr_man.txt") and as RTF ("bbr_man.rtf")
file.
The source-code is written in C, and the necessary compiling-commands differ
from system to system. You must in any case use the mathematics library,
because the program is calculating square-roots. On an SGI-workstation, the
necessary command is:
cc -lm BBReader.c
-o BBReader.exe
On a HP9000/735, running under HP-UX, the necessary command is:
cc -A a BBReader.c
-lm -o BBReader.exe
If you are working on a different kind of system, you have to find out your
specific compiling-command by means of the compiler manual.
BB-Reader is designed for protein-chemists dealing with NMR or for NMR-spectroscopists working on proteins. Given chemical shift
data the program searches for possible assignments. Given peak positions
BB-Reader suggests assingments for user-specified
homo- and heteronuclear one-to three dimensional COSY
and NOESY-type experiments. It can handle 1H, 13C and 15N
shift-data. Distance-information from PDB-files can be utilized for filtering
possible NOESY-cross-peak assignments. BBReader will
provide you with a list of possible assignments along with a ranking to give
you help for the final decision.
The basic condition is, that the assignment of the NMR-signals of the protein
you are dealing with, is known, and that the assignement
is contained in the BioMagResBank (Seavey et al. 1991) (http://www.bmrb.wisc.edu) in the STAR
flat-file-format (Hall 1991; Hall and Spadaccini
1994; Hall and Cook 1995) . Pay attention to the
experimental conditions under which the assignment was done (pH, temperature,
solvent,...)! You have to download the file to your
own computer. If you plan to work with NOESY-spectra, it is recommended (but
not necessary) that you also download the PDB-file of that protein from the
Brookhaven database (Abola et al., 1987; Bernstein et
al., 1977) (http://www.pdb.bnl.gov).
BB-Reader can work with PDB-files in the current format, only the lines
beginning with ATOM are used.
After starting the program by entering BBReader, you are prompted for
the name of the BioMagRes-file. The program will scan
the file to obtain assignment information. BB-Reader can work with 1H,
13C and 15N-shift-data.
Then you will be asked for the number of dimensions your spectrum has, you can enter
a number from 1 to 3. Version 2.0 cannot treat 4D and 5D-spectra, but you can
work around that (see section "Limitations").
You will be prompted for the nucleus for each dimension (this question is
suppressed, if data for only one nucleus is available). You are free to enter
any combination of nuclei, and BB-Reader will not refuse any, it will, however,
warn you, if you enter highly unusual combinations (e.g. NN-correlations).
All coherence transfers between 1H and 13C or 15N,
respectively, will be considered to be of COSY-type (i.e. to be based on scalar
coupling), for coherence transfers between two proton-dimensions you will be
asked, whether the coherence transfer is of COSY or of NOESY-type.
If you have a NOESY-step in your sequence, the name of a PDB-file will be
requested. The PDB-file will be used to calculate internuclear
distances and to create a distance-dependent score. This possibility is
optional, you may just enter "0", if there is no PDB-file available
or if you don't want to use it.
After the setup described above, you will be asked for the output-type you
wish. There are two possibilities:
- "single-peak-mode": you enter the position of a cross-peak (i.e.
one chemical shift per dimension) and BB-Reader will provide you with an
ordered list of those possible cross-peaks, that come closest to your input;
- "range-mode": you enter a shift-range for each dimension, and
BB-Reader will give you a list of all possible cross-peaks, that fall into that
range.
If you have specified a PDB-file and are working in "range-mode", you
will also be asked for a distance threshold - a maximum distance, above that
proton-pairs are not listed in the result-list any more.
After you having defined the characteristics of spectrum and output, BB-Reader
will search the database for nuclei with matching chemical shifts, those
potential cross-peaks are checked, whether they are possible from the
spectroscopic viewpoint. If they pass the test, they will be marked for output.
In the single-peak-mode the score is calculated and this "hit" will
be written to its place in the temporary hitlist.
The output line follows the general format:
r1 no1 at1
s1 | r2 no2 at2 s2 | t12
| r3 no3 at3 s3 | t23 |
score
the symbols mean (with subscripts referring to the spectral dimension):
r: three-letter-code for residue
no:sequence number of residue
at: atom-code as given in the BioMagResBank (see
section "Nomenclature
of atom-types" below for a detailed explanation)
t12: additional information: for a COSY-type spectrum either "geminal" for a 2J-coupling between protons
or "allylic" for a 4J-coupling
between protons is given, otherwise this field is left empty. For a
NOESY-spectrum the internuclear distance between the
two atoms [�] is printed there. If one or both coupling partners belong to a
group (see section "Groups of
equivalent atoms / ambigous assignment"
below), the shortest distance between any two atoms of that group is given.
t23: same as t12, but for dimension two and three.
score: only if single-peak-mode is chosen.
Finally BB-Reader gives information on what fraction of all nuclei in the
protein is contained in the BioMagResBank-file.
For many pairs of diastereotopic protons the stereospecific assignment is not known. Therefore two
possible assignments exist for each chemical shift. These nuclei are combined
to a group, and the shift is assigned to that group. In the output the group is
given (e.g. "HB2/HB3") instead of giving two separate assignments or
just giving only one.
Combining equivalent atoms to groups reduces the output and improves the
clarity. In case of a NOESY-type-spectrum, the shortest distance between any
members of the two groups will be given in the output.
Other isochronous atoms (e.g. HD1/HD2 in Phe and Tyr) are treated in the same way.
The three equivalent atoms of methyl groups form a "natural" group.
The score, which is used for the ranking of the hits, is calculated in the
following way:
A distance-penalty is calculated for each NOESY-step (provided that a PDB-file
was used). For distances below 4� no penalty is calculated. If the distance is
above 4�, the distance penalty is calculated as
k*(distance-4�)2 in order to make such
relatively big distances even more unlikely (k was determined empirically). If
there are two NOESY-steps, the distance-penalties for each step are added.
A shift-penalty is calculated for each dimension in the following way: shift
penalty=(f*(experimental shift - database shift))2,
f being a nucleus-dependent factor.
All shift penalties and distance penalties are added and the sum is divided by
the number of dimensions. This is to account for the fact,
that the sum of penalty points increases automatically with the number of
dimensions. This penalty is then subtracted from 100 to yield the final score.
The calculation of the score is highly empirical, and it might be subject to
future changes.
The nomenclature of atomtypes is equivalent to that
given in the BioMagResBank, it can be looked up at http://www.bmrb.wisc.edu/Nomenclature/commonaa.html.
This file contains the amino-acids along with the atom-types of all atoms as
they are given by the BioMagResBank and in the output
of BB-Reader.
BB-Reader offers the possibility for having a logfile
written. The logfile will contain all settings and
the result. The logfile is always named "RBMlog.out", it is a
text-file.
BB-Reader allows you to write a default print-command into a text-file called
"RBM_default_printcmd". This file must be
in the same directory as the program. If you have not specified a print command
"lp RBMlog.out"
will be used.
Before the program exits, it asks you, whether you'd like to have the logfile printed. You can as well specify an editor-command
like "jot RBMlog.out"
or "vi RBMlog.out".
Typically, one has many cross-peaks to examine from one spectrum. To prevent
being prompted for the same input every time you start the program for
examining a new cross-peak, several command-line-arguments are possible:
The generalized syntax is:
BBReader [-hdrlfp123] [spectrum]
The first argument can contain:
h (Help) overview about the available arguments
d (Default) the same BioMagResBank-file and the same
PDB-file as last time you ran the program are used again.
r (Ranking) single-peak-mode
l (List) range-mode
f (File) the logfile is written
p (Print) the logfile is written and printed
1 1D-spectrum
2 2D-spectrum
3 3D-spectrum
"1","2" and "3" as well as "r" and
"l" are mutually exclusive.
The second command-line-argument ("spectrum") can be used to specify
the nuclei and the coherence transfer-modes. It must be of the following
format: the first letter must be "H", "C" or "N"
and represents the nucleus of the first dimension. For 1D-spectra, the argument
must end here, for more-dimensional spectra, the
second letter must be "c" or "n" and represents the
coherence-transfer-mode between dimension one and two (COSY or NOESY). The
third letter must be the nucleus of the second dimension. If the spectrum is
three-dimensional, then another letter for the coherence transfer between
dimension 2 and 3 and another letter for the nucleus in dimension 3 is
necessary.
For example: "BBReader -3 HnHcC "
means, that the spectrum is a 3D-H-H-C spectrum with a NOESY-type-transfer
between dimension one and two and a COSY-type-transfer between dimension two
and three.
4D-spectra:
Version 2.0 of BB-Reader is restricted to 1D, 2D and 3D-spectra. Future
versions may extend this. For the time being, you can handle more than three
dimensions by performing a database-search with the first three and one search
with the last three dimensions and combine those (3D) cross-peaks, that have
the same two atoms once in dimension two and three and once in dimension one
and two.
For example, to simulate a 4D-H-C-C-H-experiment, make a search for two
3D-experiments, one being H-C-C and one being C-C-H. Then combine those
cross-peaks from both output lists, whose second and third atoms in the first
experiment are the same as the first and second atoms in the second experiment.
2D-TOCSY:
Version 2.0 contains only COSY and NOESY-type coherence transfers. You can
combine several COSY-steps in order to simulate a TOCSY. The number of
COSY-steps necessary to cover all possibilties
depends on the residue and reaches a maximum of 5 for lysine.
Amino-Acids:
Version 2.0 is restricted to the 20 classical amino-acids in the L-isomeric
form. Other amino-acids will be ignored and the user will be informed about
their occurrance.
No software is completely bug-free. If you find a bug, please send a message to
the address mentioned below.
If you have suggestions on how to improve the program or other remarks (such as
fan-post, for example (flames are piped to /dev/null)), send a message to:
Reinhard Wimmer
Department of
Sohngaardsholmsvej 49
DK-9000
Aalborg, June 2004
Abola,
E.E., Bernstein, F.C., Bryant, S.H., Koetzle, T.F.
and Weng, J. (1987). In Crystallographic
Databases - Information Content, Software Systems, Scientific Applications:
Protein Data Bank, (Eds. F.H. Allen, G. Berghoff and
R. Sievers), Data Commission of the International
Union of Crystallography, Bonn/Cambridge/Chester, pp. 107-132
Bernstein, F.C., Koetzle, T.F., Williams, G.J.B.,
Meyer, E.F.Jr., Brice, M.D., Rodgers, J.R., Kennard,
O., Shimanouchi, T. and Tasumi,
M. (1977), J. Mol. Biol., 112, 535-542
Hall, S. R. (1991) J. Chem. Inf. Comput. Sci., 31, 326-333.
Hall, S. R. and Cook, A. P. F. (1995) J. Chem. Inf. Comput. Sci., 35, 819-825.
Hall, S. R. and Spadaccini, N.
(1994) J. Chem. Inf. Comput. Sci., 34, 505-508.
Seavey, B.
R., Farr, E. A., Westler, W. M. and Markley, L.
(1991) J. Biomol. NMR, 1, 217-236.