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PdbStat: <br> <onlyinclude> | PdbStat: <br> <onlyinclude> | ||
rea coo pdb [filename] #read file with concatenated CNS pdb files | rea coo pdb [filename] #read file with concatenated CNS pdb files | ||
all | all #select all the models | ||
class | class #classify the models by energy | ||
order 0.9 | order 0.9 #determine ordered residues; phi/psi cut-off 0.9 | ||
rmsd best backbone | rmsd best backbone #backbone rmsd | ||
[return] | [return] #creates an rmsd output file | ||
write coo pdb [overlayed file] | write coo pdb [overlayed file] #write overlayed coordinates</onlyinclude> | ||
Next, open the overlayed coordinates in Molmol and get the desired rotation. Use <tt>writetransform</tt> command to write the rotation matrix to a file. <br> Back in PdbStat: <br> <onlyinclude>rea coo pdb [overlayed.pdb] #read the overlayed coordinates (all models) | Next, open the overlayed coordinates in Molmol and get the desired rotation. Use <tt>writetransform</tt> command to write the rotation matrix to a file. <br> Back in PdbStat: <br> <onlyinclude>rea coo pdb [overlayed.pdb] #read the overlayed coordinates (all models) | ||
rotate file [filename] | rotate file [filename] #apply rotation matrix | ||
write coo pdb [final.pdb] | write coo pdb [final.pdb] #write new coordinates | ||
to iupac | to iupac #converts atom nomenclature to IUPAC | ||
write coo pdb [final_iupac.pdb] | write coo pdb [final_iupac.pdb] #write IUPAC coordinates for RPF analysis</onlyinclude> | ||
==== Selecting specific models / residues / atoms. ==== | ==== Selecting specific models / residues / atoms. ==== | ||
Revision as of 18:59, 31 October 2009
PdbStat
INTRODUCTION
The PdbStat program, written and actively developed by our colleague Roberto Tejero (Universita de Valencia), is routinely used in the Montelione lab for the analysis, conversion, and manipulation of coordinate and constraint files for protein structure determination. The program is also an integral component of the Protein Structure Validation Software package (Ref. 1) used across the NESG consortium.
The current version of the software is PdbStat 5.1 (July, 2008). There is no separate publication for PdbStat; we cite this program using Bhattacharya et al, 2007 (Ref. 1). Also, there is no official manual for the program. Below are a number of basic stand-alone PdbStat commands and common uses. Going forward, we can continue to add to this document as more applications are developed.
Anyone interested in obtaining the latest version of PdbStat can contact Roberto at: roberto.tejero@uv.es
COMMANDS AND APPLICATIONS
Starting the program
pdbstat
Menu of Commands
menu gives a list of commands and keywords recognized by PdbStat (also get this using the command: help command)
Here are the recognized PdbStat commands for version 5.1:
PdbStat> menu Commands/Keywords currently recognized by PDBSTAT The commands/keywords currently recognized by PDBSTAT are given below. Type "help <command>" for more information on each PDBSTAT function. align analyze author bye class clear close chain check chiral delete debug dump energy evaluate find fit fix get help history hydrogen hyper kabsch ident/chain info initialize log/change load menu missing order phi quit rama read relax reset restore rotate save see set show rmsd to trans version what write homology commands: get change homology homa Other kind/commands/keywords of help codes(amino codes) amino(amino geometry)</onlyinclude>
Help documents for specific commands
Each command has a short help document describing its usage and options.
Syntax:
help {topic} {subtopic}
Example: PdbStat> help read
Read Syntax: rea[d] {<arg1>} {<arg2>} {<arg3>}
arg1 can be: coo[rdinates] or con[straints] or seq[uence]
arg2 can be: pdb or con[gen] or cha[rmm] or dis[man]
arg3 can be: the name of the file.
Examples: read coord pdb filename.pdb
read seq filename
read cons congen filename
read cons diana filename
Read coordinates/constraints/sequence in specified format from file. This command is able to open the file read it locating the number of structures stored and then read them.
The user needs to type only <read> then a interactive cycle with questions begins. The program offers the different formats available, so after read is typed the program offers <coords/cons/seq> and then after that the program offers the different formats <pdb,disman,....>
Preparation of final CNS coordinates for PDB deposition
Before we deposit our final coordinates we would like to order our models in order of lowest conformation energy. Also, we want to perform backbone superposition of the coordinates using ordered [S(phi) + S(psi) > 1.8] residues only. Finally, we want to rotate the ensemble to a desired orientation, which will be the orientation that appears when a user downloads out coordinates from the Protein Data Bank (www.rcsb.org). The final coordinates are saved in the original (CNS) format and IUPAC format for RPF analysis (Ref. 2).
To prepare the final coordinates file for PDB deposition use the following protocol:
PdbStat:
rea coo pdb [filename] #read file with concatenated CNS pdb files all #select all the models class #classify the models by energy order 0.9 #determine ordered residues; phi/psi cut-off 0.9 rmsd best backbone #backbone rmsd [return] #creates an rmsd output file write coo pdb [overlayed file] #write overlayed coordinates
Next, open the overlayed coordinates in Molmol and get the desired rotation. Use writetransform command to write the rotation matrix to a file.
Back in PdbStat:
rea coo pdb [overlayed.pdb] #read the overlayed coordinates (all models)
rotate file [filename] #apply rotation matrix write coo pdb [final.pdb] #write new coordinates to iupac #converts atom nomenclature to IUPAC write coo pdb [final_iupac.pdb] #write IUPAC coordinates for RPF analysis
Selecting specific models / residues / atoms.
A powerful option in PdbStat is the ability to select specific residues and/or atoms for further analysis. This is extremely useful for superposition and RMSD evaluation of selected residues/atoms.
Syntax and Examples:
#syntax
sel[ect] {model(s)} {residue(s)} {atom(s)}
#select backbone atoms of residues 5-25,30-50 in models 1,3-5,7-10
sele 1,3-5,7-10 5-25,30-50 backbone
#select N,C,CA,O atoms of residues 5-50 in all models
sele * 5-50 n,c,ca,o
#combine selection with superposition
sele * 5-50,60-85 *
rmsd sele backbone
Conversion of coordinate and constraint formats
In the course of a structure refinement we regularly have to convert between different coordinate and constraint formats for different structure programs (i.e., CYANA, XPLOR/CNS, ECEPP). We routinely use PdbStat for this.
Examples:
# converting CYANA to XPLOR/CNS coordinates:
rea coor pdb [CYANA.pdb] #read CYANA models (all)
to xplor #converts to xplor; fixes stereospecfic labels
write #answer questions
> WRITER: Output file name ?:_ 4cns.pdb
> WRITER: Coords, constraints, aco or sequence file? :_ coor
> WRITER: ... backbone, heavy, full set? (back/heavy/all/select): all
> WRITER: What model ?_ : all
> WRITER: -- All models to be written
> COORD_writer: Format (pdb/congen/RasMol) ? : pdb
- converting CYANA to XPLOR/CNS distance constraints:
rea coor pdb [CYANA.pdb] #read CYANA models; you have to read in a pdb or sequence file before the constraints
rea cons cyana [CYANA.upl] #read CYANA upls file
write #write to CNS format; add 10% to upper bound;make lower bound van der Waals (1.8 A)
> WRITER: Output file name ?:_ 4cns_noe.tbl
> WRITER: Coords, constraints, aco or sequence file? :_ cons
> WRITER_constr: Output format
[congen||discover||ecepp||disman||dyana||cyana||diana||xplor||cns]? : cns
> XPLOR_writer: percentage range for upper bound (upp+range)?: 10 > XPLOR_writer: range for lower bound (low-range)?: vdw > XPLOR_writer: ... writing ... wait
- converting CYANA to XPLOR/CNS dihedral constraints:
rea aco cyana [CYANA.aco]
write
> WRITER: Output file name ?:_ 4cns_dihe.tbl
> WRITER: Coords, constraints, aco or sequence file? :_ aco
> WRITER_constr: Output format (congen || discover || impact || disman || diana || xplor || cns)? : cns
Constraint Violations
One can analyze constraint violations using PdbStat. It is best to convert the coordinates and constraints to IUPAC format; this is the approach used internally within PSVS.
Commands:
rea coo pdb [filename] to iupac #convert coordinates to IUPAC format rea cons [format] [filename] #read distance constraints; specify format noe to iupac #convert distance constraints to IUPAC rea aco [format] [filename] #read dihedral constraints; specify format set cutu 0.2 #set cut-off for distance violations to 0.2 A see viol noe [sum/ave/center] #see noe violations using sum/average/center averaging see cutaco 1 #set cut-off for dihedral violations to 1 deg. see viol aco #see dihedral violations above threshold
Sorting of Distance Constraints
There are a number of options in PdbStat for sorting or culling distance constraints.
cons clean #keep conformationally-restricting constraints; also removes duplicates noe analysis #NOE statistics (as in PSVS) noe delete intra #delete all intra NOE constraints noe keep long #keep only long range (||i-j|| >/= 5) NOE constraints noe keep ilv #keep NOE constraints consistent with ILV labeling
Commands for Obtaining Various Metrics
The “eval”, “show”, and “see” commands allow one to evaluate several types of metrics in a structure or ensemble.
eval [procheck/rama] #get Procheck/Ramachandran statistics for model(s) eval dist * 68 sg 119 nd1 #get 68-SG to 119-ND1 distance across all models eval [phi || psi || omega] 1 #get phi/psi/omega torsion angles in model 1 see lib [residue] #see library definitions for residue type select 1 119 * #use select and see in tandem see coo #coordinates for residue 119 in model 1
Other Functions
# renumbering / resetting residue numbering
reset * 10 #sets first residue in file to 10
reset * #resets coordinates to original
# ordering ensemble using FindCore algorithm (Ref. 3):
find [ -bb || -heavy || -all || -noe ]
# contact map generation based on coordinates or constraints
contact
> DRAW_cntct: from coordinates or constraints (coor/cons) ?:_ coor
> MAIN_cntct: What model do you want (1-20) or average ?_ :ave
> do_average_coords(): Making average for backbone atoms
> do_average_coords(): Calculating center of masses
> do_average_coords(): Calling optimal rotation for backbone
> do_average_coords(): Calc. average coordinates backbone
> MAIN_cntct: distance cutoff ?:_ 4.5
> MAIN_cntct: atom type (hydr, heavy, all) ?:_ hydr #writes a postscript file
REFERENCES
1. Bhattacharya, A., Tejero, R., and Montelione, G. T. (2007) Evaluating protein structures determined by structural genomics consortia. Proteins 66, 778-795.
2. Huang, Y. J., Powers, R., and Montelione, G.T. (2005) Protein NMR Recall, Precision, and F-measure scores (RPF scores): structure quality assessment measures based on information retrieval statistics. J. Am. Chem. Soc. 127, 1665-1674.
3. Snyder, D. A. and Montelione, G. T. (2005) Clustering algorithms for identifying core atom sets and for assessing the precision of protein structure ensembles. Proteins 59, 673-686.
-- JimAramini - 14 Aug 2008