sudo pip install matplotlib scipy sklearn scikit-image protobuf psutil numpy seaborn
export PYTHONPATH=/usr/local/python:$PYTHONPATHrdkit -- see installation instructions here
openbabel -- see installation instructions here
usage: train.py [-h] -m MODEL -p PREFIX [-d DATA_ROOT] [-n FOLDNUMS] [-a] [-i ITERATIONS] [-s SEED] [-t TEST_INTERVAL] [-o OUTPREFIX] [-g GPU] [-c CONT] [-k] [-r]
[--percent_reduced PERCENT_REDUCED] [--avg_rotations] [--checkpoint] [--keep_best] [--dynamic] [--cyclic] [--solver SOLVER] [--lr_policy LR_POLICY] [--step_reduce STEP_REDUCE]
[--step_end STEP_END] [--step_end_cnt STEP_END_CNT] [--step_when STEP_WHEN] [--base_lr BASE_LR] [--momentum MOMENTUM] [--weight_decay WEIGHT_DECAY] [--gamma GAMMA]
[--power POWER] [--weights WEIGHTS] [-p2 PREFIX2] [-d2 DATA_ROOT2] [--data_ratio DATA_RATIO] [--test_only] [--clip_gradients CLIP_GRADIENTS] [--skip_full]
[--display_iter DISPLAY_ITER] [--update_ratio UPDATE_RATIO]
Train neural net on .types data.
options:
-h, --help show this help message and exit
-m MODEL, --model MODEL
Model template. Must use TRAINFILE and TESTFILE
-p PREFIX, --prefix PREFIX
Prefix for training/test files: <prefix>[train|test][num].types
-d DATA_ROOT, --data_root DATA_ROOT
Root folder for relative paths in train/test files
-n FOLDNUMS, --foldnums FOLDNUMS
Fold numbers to run, default is to determine using glob
-a, --allfolds Train and test file with all data folds, <prefix>.types
-i ITERATIONS, --iterations ITERATIONS
Number of iterations to run,default 250,000
-s SEED, --seed SEED Random seed, default 42
-t TEST_INTERVAL, --test_interval TEST_INTERVAL
How frequently to test (iterations), default 1000
-o OUTPREFIX, --outprefix OUTPREFIX
Prefix for output files, default <model>.<pid>
-g GPU, --gpu GPU Specify GPU to run on
-c CONT, --cont CONT Continue a previous simulation from the provided iteration (snapshot must exist)
-k, --keep Don't delete prototxt files
-r, --reduced Use a reduced file for model evaluation if exists(<prefix>[reducedtrain|reducedtest][num].types). Incompatible with --percent_reduced
--percent_reduced PERCENT_REDUCED
Create a reduced set on the fly based on types file, using the given percentage: to use 10 percent pass 10. Range (0,100). Incompatible with --reduced
--avg_rotations Use the average of the testfile's 24 rotations in its evaluation results
--checkpoint Enable automatic checkpointing
--keep_best Store snapshots everytime test AUC improves
--dynamic Attempt to adjust the base_lr in response to training progress, default True
--cyclic Vary base_lr in range of values: 0.015 to 0.001
--solver SOLVER Solver type. Default is SGD
--lr_policy LR_POLICY
Learning policy to use. Default is fixed.
--step_reduce STEP_REDUCE
Reduce the learning rate by this factor with dynamic stepping, default 0.1
--step_end STEP_END Terminate training if learning rate gets below this amount
--step_end_cnt STEP_END_CNT
Terminate training after this many lr reductions
--step_when STEP_WHEN
Perform a dynamic step (reduce base_lr) when training has not improved after this many test iterations, default 5
--base_lr BASE_LR Initial learning rate, default 0.01
--momentum MOMENTUM Momentum parameters, default 0.9
--weight_decay WEIGHT_DECAY
Weight decay, default 0.001
--gamma GAMMA Gamma, default 0.001
--power POWER Power, default 1
--weights WEIGHTS Set of weights to initialize the model with
-p2 PREFIX2, --prefix2 PREFIX2
Second prefix for training/test files for combined training: <prefix>[train|test][num].types
-d2 DATA_ROOT2, --data_root2 DATA_ROOT2
Root folder for relative paths in second train/test files for combined training
--data_ratio DATA_RATIO
Ratio to combine training data from 2 sources
--test_only Don't train, just evaluate test nets once
--clip_gradients CLIP_GRADIENTS
Clip gradients threshold (default 10)
--skip_full Use reduced testset on final evaluation, requires passing --reduced
--display_iter DISPLAY_ITER
Print out network outputs every so many iterations
--update_ratio UPDATE_RATIO
Improvements during training need to be better than this ratio. IE (best-current)/best > update_ratio. Defaults to 0.001MODEL is a caffe model file and is required. It should have a MolGridDataLayer for each phase, TRAIN and TEST. The source parameter of these layers should be placeholder values "TRAINFILE" and "TESTFILE" respectively.
PREFIX is the prefix of pre-specified training and test files. For example, if the prefix is "all" then there should be files "alltrainX.types" and "alltestX.types" for each X in FOLDNUMS. FOLDNUMS is a comma-separated list of ints, for example 0,1,2. With the --allfolds flag set, a model is also trained and tested on a single file that hasn't been split into train/test folds, for example "all.types" in the previous example.
The model trained on "alltrain0.types" will be tested on "alltest0.types". Each model is trained for up to ITERATIONS iterations and tested each TEST_INTERVAL iterations.
The train/test files are of the form 1 set1/159/rec.gninatypes set1/159/docked_0.gninatypes where the first value is the label, the second the receptor, and the third the ligand. Additional whitespace delimited fields are ignored. gninatypes files are created using gninatyper. The receptor and label paths in these files can be absolute, or they can be relative to a path provided as the DATA_ROOT argument. To use this option, the root_folder parameter in each MolGridDataLayer of the model file should be the placeholder value "DATA_ROOT". This can also be hard-coded into the model.
The prefix of all generated output files will be OUTPREFIX. If not specified, it will be the model name and the process id. While running, OUTPREFIX.X.out files are generated. A line is written at every TEST_INTERVAL and consists of the test auc, the train auc, the loss, and the learning rate at that iteration.
The entire train and test sets are evaluated every TEST_INTERVAL. If they are very large this may be undesirable. Alternatively, if -r is passed, pre-specified reduced train/test sets can be used for monitoring.
Once each fold is complete OUTPREFIX.X.finaltest is written with the final predicted values.
After the completion of all folds, OUTPREFIX.test and OUTPREFIX.train are written which contain the average AUC and and individual AUCs for each fold at eash test iteration. Also, a total finaltest file of all the predictions. Graphs of the training behavior (OUTPREFIX_train.pdf) and final ROC (OUTPREFIX_roc.pdf) are also created as well as caffe files.
The GPU to use can be specified with -g.
Previous training runs can be continued with -c. The same prefix etc. should be used.
A large number of training hyperparameters are available as options. The defaults should be pretty reasonable.
There are 2 strategies: 1) Running clustering.py directly; 2) Running compute_seqs.py --> compute_row.py --> combine_rows.py. Strategy 1 works best when there is a small number of training examples (around 4000), but the process is rather slow. Strategy 2 is to upscale computing the clusters (typically for a supercomputing cluster) where each row would correspond to 1 job.
Note that these scripts assume that the input files point to a relative path from the current working directory.
usage: clustering.py [-h] [--pdbfiles PDBFILES] [--cpickle CPICKLE] [-i INPUT]
[-o OUTPUT] [-c CHECK] [-n NUMBER] [-s SIMILARITY]
[-s2 SIMILARITY_WITH_SIMILAR_LIGAND]
[-l LIGAND_SIMILARITY] [-d DATA_ROOT] [--posedir POSEDIR]
[--randomize RANDOMIZE] [-v] [--reduce REDUCE]
create train/test sets for cross-validation separating by sequence similarity
of protein targets and rdkit fingerprint similarity
optional arguments:
-h, --help show this help message and exit
--pdbfiles PDBFILES file with target names, paths to pbdfiles of targets,
paths to ligand smile (separated by space)
--cpickle CPICKLE cpickle file for precomputed distance matrix and
ligand similarity matrix
-i INPUT, --input INPUT
input .types file to create folds from, it is assumed
receptors in pdb named directories
-o OUTPUT, --output OUTPUT
output name for clustered folds
-c CHECK, --check CHECK
input name for folds to check for similarity
-n NUMBER, --number NUMBER
number of folds to create/check. default=3
-s SIMILARITY, --similarity SIMILARITY
what percentage similarity to cluster by. default=0.5
-s2 SIMILARITY_WITH_SIMILAR_LIGAND, --similarity_with_similar_ligand SIMILARITY_WITH_SIMILAR_LIGAND
what percentage similarity to cluster by when ligands
are similar default=0.3
-l LIGAND_SIMILARITY, --ligand_similarity LIGAND_SIMILARITY
similarity threshold for ligands, default=0.9
-d DATA_ROOT, --data_root DATA_ROOT
path to target dirs
--posedir POSEDIR subdir of target dirs where ligand poses are located
--randomize RANDOMIZE
randomize inputs to get a different split, number is
random seed
-v, --verbose verbose output
--reduce REDUCE Fraction to sample by for reduced files. default=0.05INPUT is a types file that you want to create clusters for
Either CPICKLE or PDBFILES needs to be input for the script to work.
PDBFILES is a file of target_name, path to pdbfile of target, and path to the ligand smile (separated by space) CPICKLE is either the dump from running clustering.py one time, or the output from Case 2 (below) and allows you to avoid recomputing the costly protein sequence and ligand similarity matrices needed for clustering.
When running with PDBFILES, the script will output PDBFILES.pickle which contains (distanceMatrix, target_names, ligansim), where distanceMatrix is the matrix of cUTDM2 distance between the protein sequences, target_names is the list of targets, and ligandsim is the matrix of ligand similarities.
When running with CPICKLE, only the new .types files will be output.
A typical usage case would be to create 5 different seeds of 5fold cross-validation. First, we create seed0, which also will compute the matrices needed. This depends on having INPUT a types file that we want to generate clusters for PDBFILES (target_name path_to_pdb_file path_to_ligand_smile) for each target in types
clustering.py --pdbfiles my_info --input my_types.types --output my_types_cv_seed0_ --randomize 0 --number 5Next we run the following four commands to generate the other 4 seeds
clustering.py --cpickle matrix.pickle --input my_types.types --output my_types_cv_seed1_ --randomize 1 --number 5
clustering.py --cpickle matrix.pickle --input my_types.types --output my_types_cv_seed2_ --randomize 2 --number 5
clustering.py --cpickle matrix.pickle --input my_types.types --output my_types_cv_seed3_ --randomize 3 --number 5
clustering.py --cpickle matrix.pickle --input my_types.types --output my_types_cv_seed4_ --randomize 4 --number 5First, we will use the compute_seqs.py to generate the needed input files
usage: compute_seqs.py [-h] --pdbfiles PDBFILES [--out OUT]
Output the needed input for compute_row. This takes the format of
"<target_name> <ligand smile> <target_sequence>" separated by spaces
optional arguments:
-h, --help show this help message and exit
--pdbfiles PDBFILES file with target names, paths to pbdfiles of targets,
and path to smiles file of ligand (separated by space)
--out OUT output file (default stdout)
PDBFILES is the same input that would be given to clustering.py.
For the rest of this pipeline, I will consider the output of compute_seqs.py to be comp_seq_out.
Second, we will run compute_row.py for each line in the output of compute_seqs.py
usage: compute_row.py [-h] --pdbseqs PDBSEQS -r ROW [--out OUT]
Compute a single row of a distance matrix and ligand similarity matrix from a
pdbinfo file.
optional arguments:
-h, --help show this help message and exit
--pdbseqs PDBSEQS file with target names, ligand smile, and sequences
(chains separated by space)
-r ROW, --row ROW row to compute
--out OUT output file (default stdout)
Here PDBSEQS is the output of compute_seqs.py. For example, to compute row zero and store the output into the file row0:
compute_row.py --pdbseqs comp_seq_out --row 0 --out row0For the next part, I assume that the output of compute_row.py is row[num] where [num] is the row that was computed.
Third, we will run combine_rows.py to create the cpickle file needed for input into clustering.py
combine_rows.py row*combine_rows.py accepts any number of input files, and outputs matrix.pickle
Lastly, we run clustering.py as follows
clustering.py --cpickle matrix.pickle --input my_types.types --output my_types_cv_There are 4 scripts here which form a pipeline to generate new counter-examples for a data directory.
The pipeline is as follows: 1) generate_unique_lig_poses.py; 2) counterexample_generation_jobs.py; 3) generate_counterexample_typeslines.py; 4) types_extender.py.
Global Assumptions: 1) The data directory structure is:
<ROOT>/<POCKET>/<FILES>
```,
2) Crystal ligand files are named:<PDBid>_<ligname><CRYSTAL SUFFIX>
```,
3) Receptors are PDB files, 4) output poses are SDF files.In order to avoid extra calculations, we need to find the unique poses. NOTE - This process needs to be done exactly once when generating new counterexamples. After a round of counterexamples are generated, script 3 in the pipeline will generate the updated unique_poses.sdf file.
WARNING -- this script performs an O(n^2) calcualtion for each unique ligand name in the pocket!!
This can cause this to run very slowly if there are many receptors for the ligand to be docked into. It also can cause problems if there are many crystal ligands for 1 ligand name. In this case, we recommend creating a subdirectory for that pocket, and putting the extra crystal ligand files there.
usage: generate_unique_lig_poses.py [-h] -p POCKET -r ROOT [-ds DOCKED_SUFFIX]
[-cs CRYSTAL_SUFFIX] -os OUT_SUFFIX
[--unique_threshold UNIQUE_THRESHOLD]
Create ligname<OUTSUFFIX> files for use with generate_counterexample_typeslines.py.
optional arguments:
-h, --help show this help message and exit
-p POCKET, --pocket POCKET
Name of the pocket that you will be generating the
file for.
-r ROOT, --root ROOT PATH to the ROOT of the pockets.
-ds DOCKED_SUFFIX, --docked_suffix DOCKED_SUFFIX
Expression to glob docked poses. These contain the
poses that need to be uniqified. Default is
"_tt_docked.sdf"
-cs CRYSTAL_SUFFIX, --crystal_suffix CRYSTAL_SUFFIX
Expression to glob the crystal ligands. Default is
"_lig.pdb"
-os OUT_SUFFIX, --out_suffix OUT_SUFFIX
End of the filename for LIGNAME<OUTSUFFIX>. This will
be the --old_unique_suffix for
generate_counterexample_typeslines.py.
--unique_threshold UNIQUE_THRESHOLD
RMSD threshold for unique poses. IE poses with RMSD >
thresh are considered unique. Defaults to 0.25.The workflow for this script is to first generate a list of the pockets that you wish to analyze. We provide the pockets used for our CrossDocked2020 models in cd2020_pockets.txt.
You can then run the script in a bash for loop:
for d in `cat cd2020_pockets.txt` do python3 generate_unique_lig_poses.py -p $d -r MYROOT -os _initial_unique.sdf; doneWARNING -- this will be VERY SLOW. We HIGHLY RECOMMEND running this in a parallel fashion on a super computing cluster if possible.
The output when completed will be a series of LIGNAME_initial_unique.sdf files in each pocket directory.
We need to create the gnina commands to generate the new counterexample poses.
usage: counterexample_generation_jobs.py [-h] -o OUTFILE [-r ROOT]
[-ri REC_ID] [-cs CRYSTAL_SUFFIX]
[-ds DOCKED_SUFFIX] -i ITERATION
[--num_modes NUM_MODES] [--cnn CNN]
[--cnn_model CNN_MODEL]
[--cnn_weights CNN_WEIGHTS]
[--seed SEED] [--dirs DIRS]
Create cnn_minimize jobs for a dataset. Assumes dataset file structure is
<ROOT>/<Identifier>/<FILES>
optional arguments:
-h, --help show this help message and exit
-o OUTFILE, --outfile OUTFILE
Name for gnina job commands output file.
-r ROOT, --root ROOT ROOT for data directory structure. Defaults to current
working directory.
-ri REC_ID, --rec_id REC_ID
Regular expression to identify the receptor PDB.
Defaults to ...._._rec.pdb
-cs CRYSTAL_SUFFIX, --crystal_suffix CRYSTAL_SUFFIX
Expresssion to glob the crystal ligand PDB. Defaults
to _lig.pdb. Assumes filename is
PDBid_LignameLIGSUFFIX
-ds DOCKED_SUFFIX, --docked_suffix DOCKED_SUFFIX
Expression to glob docked poses. These contain the
poses that need to be minimized. Default is
"_tt_docked.sdf"
-i ITERATION, --iteration ITERATION
Sets what iteration number we are doing. Adds
_it#_docked.sdf to the output file for the gnina job
line.
--num_modes NUM_MODES
Sets the --num_modes argument for the gnina command.
Defaults to 20.
--cnn CNN Sets the --cnn command for the gnina command. Defaults
to dense. Must be dense, general_default2018, or
crossdock_default2018.
--cnn_model CNN_MODEL
Override --cnn with a user provided caffe model file.
If used, requires the user to pass in a weights file
as well.
--cnn_weights CNN_WEIGHTS
The weights file to use with the supplied caffemodel
file.
--seed SEED Seed for the gnina commands. Defaults to 42
--dirs DIRS Supplied file containing a subset of the dataset (one pocket per line).
Default behavior is to do every directory.The default behavior is to generate the output file for each directory in ROOT. For CrossDocked2020, we supply more pockets than we used to analyze, so you can pass the cd2020_pockets.txt file in the DIRS argument. The default values match what we used for CrossDocked2020.
Example -- generate the file it3_to_run.txt for CrossDocked2020 available at my_root for iteration 3, using the built-in dense net in gnina
python3 counter_example_generation_jobs.py -o it3_to_run.txt -r MYROOT -i 3 --cnn dense --dirs cd2020_pockets.txtOnce this has been created, each of these commands will need to be executed. Note, there will be many commands to run, so we recommend running in parallel across many GPUs on a computing cluster if possible.
Running this script will generate OUTNAME in the supplied pocket, which will contain the lines to add to the types files for that pocket.
WARNING -- This script also performs an O(n^2) calculation per unique ligand in the pocket! This can take a very long time, and scales with the number of receptors and crystal ligands with the same ligand name present in the pocket. If this is to much, we recommend a downsampling strategy by moving files into a sub-directory prior to running the pipeline.
WARNING 2 -- As the calculations are O(n^2), we recommend running each pocket as its own job on a computing cluster if possible.
usage: generate_counterexample_typeslines.py [-h] -p POCKET -r ROOT -i INPUT
[-cs CRYSTAL_SUFFIX]
[--old_unique_suffix OLD_UNIQUE_SUFFIX]
[-us UNIQUE_SUFFIX]
[--unique_threshold UNIQUE_THRESHOLD]
[--lower_confusing_threshold LOWER_CONFUSING_THRESHOLD]
[--upper_confusing_threshold UPPER_CONFUSING_THRESHOLD]
[--good_pose_thresh GOOD_POSE_THRESHOLD]
[--bad_pose_thresh BAD_POSE_THRESHOLD]
-o OUTNAME [-a AFFINITY_LOOKUP]
Create lines to add to types files from counterexample generation. Assumes
data file structure is ROOT/POCKET/FILES.
optional arguments:
-h, --help show this help message and exit
-p POCKET, --pocket POCKET
Name of the pocket that you will be generating the
lines for.
-r ROOT, --root ROOT PATH to the ROOT of the pockets.
-i INPUT, --input INPUT
File that is output from
counterexample_generation_jobs.py
-cs CRYSTAL_SUFFIX, --crystal_suffix CRYSTAL_SUFFIX
Expresssion to glob the crystal ligand PDB. Defaults
to _lig.pdb. Needs to match what was used with
counterexample_generation_jobs.py
--old_unique_suffix OLD_UNIQUE_SUFFIX
Suffix for the unique ligand sdf file from a previous
run. If set we will load that in and add to it.
Default behavior is to generate it from provided input
file.
-us UNIQUE_SUFFIX, --unique_suffix UNIQUE_SUFFIX
Suffix for the unique ligand sdf file for this run.
Defaults to _it1___.sdf. One will be created for each
ligand in the pocket.
--unique_threshold UNIQUE_THRESHOLD
RMSD threshold for unique poses. IE poses with RMSD >
thresh are considered unique. Defaults to 0.25.
--lower_confusing_threshold LOWER_CONFUSING_THRESHOLD
CNNscore threshold for identifying confusing good
poses. Score < thresh & under 2RMSD is kept and
labelled 1. 0<thresh<1. Default 0.5
--upper_confusing_threshold UPPER_CONFUSING_THRESHOLD
CNNscore threshold for identifying confusing poor
poses. If CNNscore > thresh & over 2RMSD pose is kept
and labelled 0. lower<thresh<1. Default 0.9
--good_pose_thresh GOOD_POSE_THRESH
RMSD threshold to identify a good pose.
If ligand RMSD to crystal < this value, the pose
is labeled bad. Defaults to 2.0.
--bad_pose_thresh BAD_POSE_THRESH
RMSD threshold to identify a bad pose.
If ligand RMSD to crystal >= this value, the pose
is labeled bad. Defaults to 2.0.
-o OUTNAME, --outname OUTNAME
Name of the text file to write the new lines in. DO
NOT WRITE THE FULL PATH!
-a AFFINITY_LOOKUP, --affinity_lookup AFFINITY_LOOKUP
File mapping the PDBid and ligname of the ligand to
its pK value. Assmes space delimited "PDBid ligname
pK". Defaults to pdbbind2017_affs.txtExample -- finishing the pipeline from the previous examples for ZIPA_ECOLI_187_328_0
python3 generate_counterexample_typeslines.py -p ZIPA_ECOLI_187_328_0 -r MYROOT -i it3_to_run.txt -us _it3___.sdf -o it3_typeslines_toadd.txt --old_unique_suffix _initial_unique.sdfThe above command will be need to run for each directory in cd2020_pockets.txt. It will create the it3_typeslines_toadd.txt in the pocket directory.
That text file contains the lines that need to be added to the training/test types files. The default values match what we used for the CrossDocked2020 paper.
Now that the lines we need to add are generated for each pocket, we can run types_extender.py on each of the types files that we use for training and testing to generate new types files with these added lines.
usage: types_extender.py [-h] -i INPUT -o OUTPUT -n NAME [-r ROOT]
Add lines to types file and create a new one. Assumes data file structure is
ROOT/POCKET/FILES.
optional arguments:
-h, --help show this help message and exit
-i INPUT, --input INPUT
Types file you will be extending.
-o OUTPUT, --output OUTPUT
Name of the extended types file.
-n NAME, --name NAME Name of the file containing the lines to add for a
given pocket. This is the output of
generate_counterexample_typeslines.py.
-r ROOT, --root ROOT Root of the data directory. Defaults to current
working directory.Continuing our example, after running script 3 there will be an it3_typeslines_toadd.txt file in each pocket. So now we generate a new train types file and new test types file as below:
python3 types_extender.py -i my_initial_train.types -o my_new_train.types -n it3_typeslines_toadd.txt -r MYROOT
python3 types_extender.py -i my_initial_test.types -o my_new_test.types -n it3_typeslines_toadd.txt -r MYROOTThere are two scripts to help you visualize how the model scores atoms: 1) simple_grid_visualization.py; 2) grid_visualization.py
Script 1 fixes a single receptor atom, & places a lig atom along specified points on the Xaxis & score them. This gives insight into how the model behaves in a simplified 2D coordinate system.
Script 2 creates a cube of single atom points around a specified receptor, which are all scored. This gives insight into how the model behaves in a simplified 3D system. A glycine tripeptide is included in this directory as a starting point.
Note: both of these scripts need to be run twice in order to complete their entire function.
usage: simple_grid_visualization.py [-h] -r RECATOMS -l LIGATOMS [-o OUTNAME]
[-t TYPESROOT] -m MODEL -w WEIGHTS
[-n NUM_POINTS] [-i INCREMENT]
[-b BOX_SIZE] [--plot] [-d DATAROOT]
Script for generating the jobs that need to be run for simple visualization.
Generates types files & a text file that needs to be run. This results in
separating atoms along the x-axis. Can then graph the results.
optional arguments:
-h, --help show this help message and exit
-r RECATOMS, --recatoms RECATOMS
File containing Receptor atom types of your modelfile
(1 per line)
-l LIGATOMS, --ligatoms LIGATOMS
File containing Ligand atom types of your modelfile (1
per line)
-o OUTNAME, --outname OUTNAME
File containing commands to be evaluated to predict
grid points. Note: Requires GNINASCRIPTSDIR to be set
environment variable. (default:
simplegrid_predicts.txt)
-t TYPESROOT, --typesroot TYPESROOT
Root folder for gninatypes data generated from script.
(default: simpletypes/)
-m MODEL, --model MODEL
Model file that predictions will be made with. Must
end in .model
-w WEIGHTS, --weights WEIGHTS
Weights for the model file that the predictions will
be made with.
-n NUM_POINTS, --num_points NUM_POINTS
Number of points. Defaults are reasonable. (default:
200)
-i INCREMENT, --increment INCREMENT
increment (Angstroms) between points. Combines with
num_points multiplicitavely. Defaults for both result
in 200 points spanning 20 angstroms (default: 0.1)
-b BOX_SIZE, --box_size BOX_SIZE
Size of the box. Used for sanity check that you are
not trying to predict outside of box for gnina. MUST
MATCH BOX OF MODEL. Defaults are default grid size for
gnina (default: 24)
--plot Flag to make 1 large plot from the data. Assumes
job(s) have completed. Requires Hydrogen to be a vaild
receptor. Saves pdf called simple_vis.pdf in the
current working directory (default: False)
-d DATAROOT, --dataroot DATAROOT
Root folder of data resulting from output of running
the OUTNAME file (default: simpledata/)The workflow for this script is the following: 1) Generate OUTNAME, 2) run each command present in OUTNAME, 3) Plot
As an example, I will use the default values of the script, RECATOMS=my_recatoms.txt, LIGATOMS=my_ligatoms.txt, MODEL=my_model.model, and WEIGHTS=my_modelweights.caffemodel.
First, we need to generate the commands to run with gnina. (this is OUTNAME, which will be simplegrid_predicts.txt)
python simple_grid_visualization.py -m my_model.model -w my_modelweights.caffemodel -r my_recatoms.txt -l my_ligatoms.txtThis will generate 2 new directories: simpledata (empty) and simpletypes. Simpleteypes should have a directory for every unique rec and lig atom. Additionally there will be a .types file for every rec+lig atom combination. Each types file should be NUM_POINTS lines (200 in this case).
Additionally, in the current working directory, there should be a new file called OUTNAME (simplegrid_predicts.txt). It will have 1 line per rec and lig atom combination.
Now we need to set the GNINASCRIPTSDIR environment variable. This would correspond to where this repo is installed.
export GNINASCRIPTSDIR=~/git/gnina/scriptsThird, we need to evaluate each line in simplegrid_predicts.txt. Note: this could take a fair amount of time on one machine, as this CANNOT be parallelized due to each job requiring the use of the GPU.
sh simplegrid_predicts.txtAfter the above command has completed, simpledata should now be populated with
python simple_grid_visualization.py -m my_model.model -w my_modelweights.caffemodel -r my_recatoms.txt -l my_ligatoms.txt --plotThis will make 1 large pdf containing all the plots, simple_vis.pdf.
usage: grid_visualization.py [-h] -r RECATOMS -l LIGATOMS [-o OUTNAME]
[-t TYPESROOT] -m MODEL -w WEIGHTS [-p TEST_PDB]
[-c CUBE_LENGTH] [-n NUM_POINTS] [--make_dx]
[-d DATAROOT]
Script for generating the jobs that need to be run for visualization.
Generates types files & a text file that needs to be run. Can make a DX file
for visualization
optional arguments:
-h, --help show this help message and exit
-r RECATOMS, --recatoms RECATOMS
File containing Receptor atom types of your modelfile (1 per line)
-l LIGATOMS, --ligatoms LIGATOMS
File containing Ligand atom types of your modelfile (1 per line)
-o OUTNAME, --outname OUTNAME
File containing commands to be evaluated to predict
grid points. Note: Requires GNINASCRIPTSDIR to be a
set environment variable. (default: grid_predicts.txt)
-t TYPESROOT, --typesroot TYPESROOT
Root folder for gninatypes data generated from script.
(default: types/)
-m MODEL, --model MODEL
Model file that predictions will be made with. Must
end in .model
-w WEIGHTS, --weights WEIGHTS
Weights for the model file that the predictions will
be made with.
-p TEST_PDB, --test_pdb TEST_PDB
pdbfile of receptor, centered at the origin for
visualization (default: gly_gly_gly.pdb)
-c CUBE_LENGTH, --cube_length CUBE_LENGTH
Width of cube for grid box of points. Defaults are
reasonable (default: 24.0)
-n NUM_POINTS, --num_points NUM_POINTS
Number of points per half of the box (ex 20 means
there will be 39x39x39 points total). Defaults are
reasonable. (default: 20)
--make_dx Flag to make dx files from the data. Assumes job(s)
have completed. (default: False)
-d DATAROOT, --dataroot DATAROOT
Root folder of data resulting from output (default:
data/)The first run of this script is WITHOUT the --make_dx flag. This will produce a file OUTNAME
wherin each line will need to be executed, and GITSCRIPTSDIR is a set environment variable which
points to the location where you have cloned this repository. The gly_gly_gly.pdb file is provided
in this directory, and is 3 connected glycine residues whose center of mass is at (0,0,0).
As before I will be evaluating the defaults of the script with RECATOMS=my_recatoms.txt, LIGATOMS=my_ligatoms.txt, MODEL=my_model.model, and WEIGHTS=my_modelweights.caffemodel. Note: gly_gly_gly.pdb needs to be in the current working directory, and the gninatyper tool needs to be installed on your machine (it is installed alongside gnina).
First we must make the textfile with all of the commands to be run with gnina.
python grid_visualization.py -m my_model.model -w my_modelweights.caffemodel -r my_recatoms.txt -l my_ligatoms.txtNext, we need to execute each command in OUTNAME (grid_predicts.txt). NOTE: this cannot be parallelized on one machine
as each commands requires the GPU to be utilized.
sh grid_predicts.txtAfter all of the lines in OUTNAME have been completed, rerun this script with the --make_dx flag
and with the same arguments as before.
python grid_visualization.py -m my_model.model -w my_modelweights.caffemodel -r my_recatoms.txt -l my_ligatoms.txt --make_dxDATAROOT will now contain the corresponding dx files. In order to visualize load the receptor and a dx file of interest
via pymol: pymol TEST_PDB my_dxfile. Visualizations can be performed by adjusting the volume slider & color of the dx object.