Set of useful HADDOCK utility scripts, which requires Python 3.7+.
This is a collection of scripts useful for pre- and post-processing and analysis for HADDOCK runs.
Requests for new scripts will be taken into consideration, depending on the effort and general usability of the script.
Download the zip archive or clone the repository with git. This last is the recommended option as it is then extremely simple to get updates.
# To download
git clone https://github.com/haddocking/haddock-tools
# To compile the executables
cd haddock-tools
make
# To update
cd haddock-tools && git pull origin masterA python script to obtain a list of passive residues providing a PDB file and a list of active residues. This will automatically calculate a list of surface residues from the PDB to filter out buried residues except if a surface list is provided. By default, neighbors of the active residues are searched within 6.5 Angstroms and surface residues are residues whose relative side chain accessibility or main chain accessibility is above 15%.
Requirements:
pip install freesasa
pip install biopython
Usage:
./passive_from_active.py [-h] [-c CHAIN_ID] [-s SURFACE_LIST]
pdb_file active_list
positional arguments:
pdb_file PDB file
active_list List of active residues IDs (int) separated by commas
optional arguments:
-h, --help show this help message and exit
-c CHAIN_ID, --chain-id CHAIN_ID
Chain id to be used in the PDB file (default: All)
-s SURFACE_LIST, --surface-list SURFACE_LIST
List of surface residues IDs (int) separated by commasA python script to create ambiguous interaction restraints for use in HADDOCK based on list of active and passive residues (refer to the HADDOCK software page for more information)
Usage:
./active-passive_to_ambig.py <active-passive-file1> <active-passive-file2>where is a file consisting of two space-delimited lines with the first line active residues numbers and the second line passive residue numbers. One file per input structure should thus be provided.
A python script to creates distance restraints to lock several chains together. Useful to avoid unnatural flexibility or movement due to sequence/numbering gaps during the refinement stage of HADDOCK.
Usage:
./restrain_bodies.py [-h] [--exclude EXCLUDE [EXCLUDE ...]] [--verbose] structures [structures ...]
positional arguments:
structures PDB structures to restraint
optional arguments:
-h, --help show this help message and exit
--exclude EXCLUDE [EXCLUDE ...], -e EXCLUDE [EXCLUDE ...] Chains to exclude from the calculation
--verbose, -vCalculates distances between neighboring residues of a ligand molecule and produces a set of unambiguous distance restraints for HADDOCK to keep it in place during semi-flexible refinement. Produces, at most, one restraint per ligand atom.
Usage:
./restrain_ligand.py [-h] -l LIGAND [-p] pdbf
positional arguments:
pdbf PDB file
optional arguments:
-h, --help show this help message and exit
-l LIGAND, --ligand LIGAND
Ligand residue name
-p, --pml Write Pymol file with restraintsThe validate_tbl.py script in that directoy will check the correctness of your restraints (CNS format) for HADDOCK.
Usage:
usage: python validate_tbl.py [-h] [--pcs] file
This script validates a restraint file (*.tbl).
positional arguments:
file TBL file to be validated
optional arguments:
-h, --help show this help message and exit
--pcs PCS mode$ python3 haddock-CSB-tools/calc-accessibility.py -h [17:06:52]
usage: calc-accessibility.py [-h] [--log-level {DEBUG,INFO,WARNING,ERROR,CRITICAL}] [--cutoff CUTOFF] pdb_input
positional arguments:
pdb_input PDB structure
optional arguments:
-h, --help show this help message and exit
--log-level {DEBUG,INFO,WARNING,ERROR,CRITICAL}
--cutoff CUTOFF Relative cutoff for sidechain accessibility
$ python3 haddock-CSB-tools/calc-accessibility.py complex_1w.pdb --cutoff 0.4 [17:10:51]
02/11/2020 17:10:57 L157 INFO - Calculate accessibility...
02/11/2020 17:10:57 L228 INFO - Chain: A - 115 residues
02/11/2020 17:10:57 L228 INFO - Chain: B - 81 residues
02/11/2020 17:10:57 L234 INFO - Applying cutoff to side_chain_rel - 0.4
02/11/2020 17:10:57 L244 INFO - Chain A - 82,83,84,85,86,87,88,90,91,94,95,98,99,102,104,106,109,113,116,117,118,122,128,129,130,132,139,141,144,145,148,149,150,151,153,156,158,160,162,163,167,168,169,170,171,173,174,175,176,178,179,180,181,183,184,186,188,194,196
02/11/2020 17:10:57 L244 INFO - Chain B - 1,2,4,5,8,11,12,15,18,21,23,24,25,26,27,30,31,33,34,37,38,41,43,44,45,46,47,50,63,64,67,69,70,73,74,76,77,78,79,80,81Converts the cluster*.pdb files in a run directory to IHM mmCIF format
Warning: Limited functionally, still work in progress! Tested for hetero-complexes with ambig restraints.
Needs ihm and biopython, install it with
$ pip install ihm --install-option="--without-ext"
$ pip install biopython$ python3 create_cif.py -h
usage: create_cif.py [-h] run_directory
positional arguments:
run_directory Location of the uncompressed run, ex:
/home/rodrigo/runs/47498-protein-protein
optional arguments:
-h, --help show this help message and exit
$ python3 haddock-CSB-tools/create_cif.py ~/projects/cif_parser/47518-cif
[23/02/2021 13:45:25] INFO Converting the cluster*.pdb structures to .cif
[23/02/2021 13:45:25] INFO Looking for models in /Users/rodrigo/projects/cif_parser/47518-cif
[23/02/2021 13:45:25] INFO Found 4 structures
[23/02/2021 13:45:25] INFO Looking for the tblfile field in /Users/rodrigo/projects/cif_parser/47518-cif/job_params.json
[23/02/2021 13:45:25] INFO tblfile field found, extracting information
[23/02/2021 13:45:25] INFO Converting /Users/rodrigo/projects/cif_parser/47518-cif/cluster1_1.pdb
[23/02/2021 13:45:26] INFO Saving as cluster1_1.cif
[23/02/2021 13:45:26] INFO Converting /Users/rodrigo/projects/cif_parser/47518-cif/cluster1_2.pdb
[23/02/2021 13:45:26] INFO Saving as cluster1_2.cif
[23/02/2021 13:45:27] INFO Converting /Users/rodrigo/projects/cif_parser/47518-cif/cluster1_3.pdb
[23/02/2021 13:45:27] INFO Saving as cluster1_3.cif
[23/02/2021 13:45:28] INFO Converting /Users/rodrigo/projects/cif_parser/47518-cif/cluster1_4.pdb
[23/02/2021 13:45:29] INFO Saving as cluster1_4.cif
A c++ program to calculate all heavy atom interchain contacts (where the chain identification is taken from the segid) within a given distance cutoff in Angstrom.
Usage:
contact-segid <pdb file> <cutoff>A c++ program to calculate all heavy atom interchain contacts (where the chain identification is taken from the chainID) within a given distance cutoff in Angstrom.
Usage:
contact-chainID <pdb file> <cutoff>A python script to predict the protonation state of Histidine residues for HADDOCK. It uses molprobity for this, calling the Reduce software which should in the path.
Usage:
./molprobity.py <PDBfile>Example:
./molprobity.py 1F3G.pdb
## Executing Reduce to assign histidine protonation states
## Input PDB: 1F3G.pdb
HIS ( 90 ) --> HISD
HIS ( 75 ) --> HISEAn optimized file is also written to disk, in this example it would be called 1F3G_optimized.pdb.
Simple perl script to remove the chainID from a PDB file
Usage:
pdb_blank_chain inputfile > outputfileSimple perl script to remove the segid from a PDB file
Usage:
pdb_blank_segid inputfile > outputfileSimple perl script to remove both the chainID and segid from a PDB file
Usage:
pdb_blank_chain-segid inputfile > outputfileSimple perl script to copy the chainID to the segid in a PDB file
Usage:
pdb_chain-to-segid inputfile > outputfileSimple perl script to copy the segid to the chainID in a PDB file
Usage:
pdb_segid-to-chain inputfile > outputfileSimple perl script to copy the chainID to segid in case the latter is empty (or vice-verse) in a PDB file
Usage:
pdb_chain-segid inputfile > outputfileSimple perl script to set the chainID in a PDB file
Usage:
pdb_setchain -v CHAIN=chainID inputfile > outputfileSimple perl script to concatenate separate single structure PDB files into a multi-model PDB file. Usage:
joinpdb -o outputfile [inputfiles]
where inputfiles are a list of PDB files to be concatenatedA python script to mutate residues for HADDOCK. A mutation list file is used as input, and the output is/are corresponding PDB file(s) of mutant(s). The format of mutation in the mutation list file is "PDBid ChainID ResidueID ResidueNameWT ResidueNameMut".
Usage:
./pdb_mutate.py <mutation list file>Example:
./pdb_mutate.py mut_1A22.list
## In mut_1A22.list, the residue 14, 18 and 21 in chain A will be mutated to ALA:
## 1A22.pdb A 14 MET ALA
## 1A22.pdb A 18 HIS ALA
## 1A22.pdb A 21 HIS ALAA python script to check format of PDB files with respect to HADDOCK format rules. A PDB file is used as input, and the output is a console message if an error or a warning is triggered by a bad formmated line. The script uses wwPDB format guidelines wwwPDB guidelines and check resid against a list of known ligands and amino-acids recognized by HADDOCK.
Usage:
./pdb_strict_format.py [-h] [-nc] pdb
This script validates a PDB file (*.pdb).
positional arguments:
pdb PDB file
optional arguments:
-h, --help show this help message and exit
-nc, --no_chainid Ignore empty chain idsA python script to transform a haddockparam.web file into a JSON structure. It is possible to use it as a class and then access
extra functions like: change_value(key, value) ; update(subdict_to_replace) ; dump_keys() ; get_value(key) ; write_json()
Usage:
./param_to_json.py [-h] [-o OUTPUT] [-g GET] [-e [EXAMPLE]] web
This script parses a HADDOCK parameter file (*.web) and transforms it to JSON
format. It also allows to change a parameter of the haddockparam.web
positional arguments:
web HADDOCK parameter file
optional arguments:
-h, --help show this help message and exit
-o OUTPUT, --output OUTPUT
Path of JSON output file
-g GET, --get GET Get value of a particular parameter
-e [EXAMPLE], --example [EXAMPLE]
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