NAME
EnumerateSmotifCombinations
VERSION
Version 0.01
SYNOPSIS
Module for enumerating combinations of Smotifs to generate full protein models
Usage:
use EnumerateSmotifCombinations;
EnumerateSmotifCombinations($pdbcode,$mot,$havestructure);
EXPORT
enumerate
full_enum
prepare_for_enumeration
pre_gen_list
gen_list
prepare_for_enumeration This subroutine prepares all the files needed for enumeration
pre_gen_list
Subroutine to generate the input list for enumeration
gen_list Subroutine to generate the input list for enumeration
enumerate
This subroutine builds a full enumeration of combinations of given smotifs (stored in a file) and calculates 4 scoring component values: radius of gyration, statistical pairwise contact potential, implicit solvation potential, and long range H bond potential.
INPUTS 1. pdbcode - the 4-character name of the folder to store input and output data 2. mot1 - an underscore-delimited set of characters outlining which subset of smotifs to enumerate. Example: If there are 4 putative smotifs, each with 5 candidates, _0_2_3 will take the first candidate for smotif1, the third candidate for smotif2, the fourth candidate for smotif3, and then enumerate through all the candidates for smotif4, resulting in 5 structures total. For the same set, _1 will take the second candidate for smotif1, and enumerate all combinations for the following three smotifs, resulting in 5x5x5=125 candidates. 3. havestructure - either 0 or 1 0 indicate there is no solved structure for comparison 1 indicate solved structure exists in the input folder. If 1, the RMSD of each enumerated structure (as compared to the solved structure) will be output, as well as GDT_TS scores for thos structures with RMSD < 10A. If the no structure option is selected (0), the RMSD and GDT_TS columns of the output will contain zeros.
REQUIRED FILES (all to be found in the "pdbcode" directory) "pdbcode".out - file containing a list of start and end points of smotifs in the query protein, as well as secondary structure and loop lengths. This is one of the standard output files of the generate_shift_files.pl script.
"pdbcode"_motifs_best.csv - file containing a list of candidates for each putative smotif.
This is one of the standard output files of the findranks.pl script.
OUTPUT (to screen) For each enumerated structure without excessive steric clashes (# backbone atoms within 2A < number of smotifs), tab-delimited information about the constituent smotifs and the overall structure scoring components is printed to the screen.
Sample line for a structure with 4 smotifs 1.437 0.740 1.867 8.377 224162 148918 54194 127698 1.7483 0.9973 0.9616 1.2306 8.8294 58.8240 12 0 0 0 0
Explanation: 1.437 0.740 1.867 8.377 : RMSDs of the 4 smotif components individually 224162 148918 54194 127698 : Nids of the 4 smotif components 1.7483 : Per-residue radius of gyration z-score 0.9973 : Per-residue pairwise contact potential z-score 0.9616 : Per-residue solvation potential z-score 1.2306 : Long-range H-bond potential z-score 8.8294 : Overall structure RMSD (from solved structure) 58.8250 : Overall structure GDT_TS score 12 0 0 0: List of indices of smotifs, as found in the <pdbcode>_motifs_best.csv file 0 : Number of steric clashes
full_enum Subroutine to recursively run full enumeration
in_array Subroutine to check if a scalar element is in an array
AUTHOR
Fiserlab Members , <andras at fiserlab.org>
BUGS
Please report any bugs or feature requests to bug-. at rt.cpan.org
, or through the web interface at http://rt.cpan.org/NoAuth/ReportBug.html?Queue=.. I will be notified, and then you'll automatically be notified of progress on your bug as I make changes.
SUPPORT
You can find documentation for this module with the perldoc command.
perldoc EnumerateSmotifCombinations
You can also look for information at:
RT: CPAN's request tracker (report bugs here)
AnnoCPAN: Annotated CPAN documentation
CPAN Ratings
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LICENSE AND COPYRIGHT
Copyright 2015 Fiserlab Members .
This program is free software; you can redistribute it and/or modify it under the terms of the the Artistic License (2.0). You may obtain a copy of the full license at:
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