PocketXMol

This is a preliminary code release for the pocket-interacting foundation model "PocketXMol".

Please note that this code is a preview version and has yet to be cleaned up and refactored. It may be hard to read but should be functional for running. We will continue to improve the code and provide more detailed instructions in the future.

This repository is modified from the MolDiff repository (a good starting point for diffusion-based molecular generation). We thank the authors for their work.

Contents

• Setup
  • Environment
  • Data and model weights
• Sample for data in test sets
  • Small molecule docking
  • Peptide docking
  • Molecular conformation generation
  • Structure-based drug design (SBDD)
  • 3D molecule generation
  • Fragment linking
  • PROTAC design
  • Fragment growing
  • De novo peptide design
  • Peptide inverse folding
• Sample for provided data
  • Basic configuration explanation
  • Customized setting explanation
• Train

Setup

Environment

To setup the environment on a Linux server, you can use Anaconda to create a new environment pxm from the environment.yml file (for CUDA 11.7) using the following commands (takes several minutes):

conda env create -f environment.yml
conda activate pxm

If you have a different CUDA version, you may need to modify the versions of the pytorch-related packages in the environment.yml file.

Data and model weights

Processed test data and model weights for sampling

For sampling, the processed data and trained model weights are included in the file data_test.tar.gz available from the Google Drive. Download and extract it using the command:

tar -zxvf data_test.tar.gz

After extraction, there will be a directory named data which contains:

• test sets: test for benchmark related information; csd for CrossDocked2020 set, geom for GEOM-Drug set, moad for Binding MOAD set, pepbdb for PepBDB set, poseboff for PoseBusters set, and protacdb for PROTAC-DB set.
• trained model weights in the trained_model directory for sampling.
• example data files (in examples directory) for demonstrating the sampling for user-provided files.

Processed data for training

For training, the demonstrative processed training data are in the file data_train_processed_reduced.tar.gz from the Google Drive. The complete processed training data are too large (>500G) so we provide a reduced subset just to demonstrate the training process. Similarly, download and extract it using the command:

tar -zxvf data_train_processed_reduced.tar.gz

Then there is a directory named data_training containing reduced training sets for demonstrative training.

Raw data and processing steps

If you want to train the model with the full training data, please follow the instructions in the process/process_steps.md file to process the raw data for complete training.

Sample for data in test sets

We provide the configuration files for sampling in the test sets of individual tasks.

NOTE:

• The batch size for sampling is defined in the configuration files. They were verified on an 80G A100 GPU. If the batch size is too large for your GPU memory, please reduce batch_size in the configuration files or directly set the batch size in the command line (e.g., --batch_size 100).
• Typical running time for individual test sets is around 1 ~ 6 hours on a single A100 GPU.
• After sampling, there will be a new directory in the specified outdir containing the generated results. The new directory is named as {exp_name}_{timestamp} where exp_name is created from the names of the configuration file and timestamp is the time when the experiment starts. Within it, the SDF subdirectory contains the generated molecules, and files gen_info.csv and log.txt contain the generation information.

Small molecule docking

Sample docking poses for 428 pairs of protein and small-molecule in the PoseBusters set.

python scripts/sample_drug3d.py \
    --config_task configs/sample/test/dock_poseboff/base.yml \
    --outdir outputs_test/dock_posebusters \
    --device cuda:0

The task configuration files are in configs/sample/test/dock_poseboff. Configuration files include:

• base.yml: dock using Gaussian noise (default)
• base_flex.yml: dock using flexible noise

• prior_center.yml: dock with prior knowledge of the molecular center
• prior_bond_length.yml: dock with prior knowledge of bond length
• prior_anchor.yml: dock with prior knowledge of approximate anchor atom coordinate
• prior_fix_anchor.yml: dock with fixed anchor atom coordinate

Confidence scores

The self-confidence scores are in the gen_info.csv file produced during the sampling process. To calculate other confidence scores for the generated molecular poses, use the following command:

python scripts/believe.py \
    --exp_name base_pxm \
    --result_root outputs_test/dock_posebusters \
    --config configs/sample/confidence/tuned_cfd.yml \
    --device cuda:0

The parameters:

• result_root is the directory containing the sampling experiments (equal to the parameter outdir of the sampling command).
• exp_name is the name of the sampling experiment directory (looks like base_pxm_20241030_225401). If there is only one experiment with the name starting with the exp_name, the appended timestamp can be omitted (i.e., set as base_pxm).
• config is the confidence model confifuration file. They are in configs/sample/confidence including:
  • tuned_cfd.yml: the tuned confidence predictor
  • flex_cfd.yml: using original model with flexible noise for confidence prediction

Ranking scores

To get the ranking scores for pose selection, after obtaining the confidence scores, use the following command:

python scripts/rank_pose.py \
    --exp_name base_pxm \
    --result_root outputs_test/dock_posebusters \
    --db poseboff

to produce the ranking.csv file which contains the self_ranking and tuned_ranking columns as ranking scores.

Peptide docking

Sample docking poses for 79 pairs of protein and peptide in the peptide docking test set.

python scripts/sample_pdb.py \
    --config_task configs/sample/test/dock_pepbdb/base.yml \
    --outdir outputs_test/dock_pepbdb \
    --device cuda:0

The task configuration files are in configs/sample/test/dockpep_pepbdb. Configuration files include:

• base.yml: dock using Gaussian noise (default)
• base_flex.yml: dock using flexible noise
• prior_fix_anchor.yml: dock with fixed anchor atom coordinate
• prior_fix_first_residue.yml: dock with fixed first residue atom coordinates
• prior_fix_terminal_residue.yml: dock with fixed both terminal residue atom coordinates
• prior_fix_backbone.yml: dock with fixed backbone atom coordinates

Molecular conformation generation

Sample molecular conformations for the 199 molecules in the conformation test set.

python scripts/sample_drug3d.py \
    --config_task configs/sample/test/conf_geom/base.yml \
    --outdir outputs_test/conf_geom \
    --device cuda:0

Structure-based drug design (SBDD)

Sample drug-like molecules for the 100 protein pockets in the SBDD test set.

python scripts/sample_drug3d.py \
    --config_task configs/sample/test/sbdd_csd/base.yml \
    --outdir outputs_test/sbdd_csd \
    --device cuda:0

The task configuration files are in configs/sample/test/sbdd_csd. Configuration files include:

• base.yml: sbdd using refine-based sampling strategy (default)
• ar.yml: sbdd using an auto-regressive-like sampling strategy
• simple.yml: sbdd with only one generation round, not using confidence scores for sampling
• base_mol_size.yml: sbdd using refine-based sampling strategy with molecular sizes determined from reference molecules

3D molecule generation

Generate drug-like molecules with the sizes as the GEOM-Drug validation set.

python scripts/sample_drug3d.py \
    --config_task configs/sample/test/denovo_geom/base.yml \
    --outdir outputs_test/denovo_geom \
    --device cuda:0

The task configuration files are in configs/sample/test/denovo_geom. Configuration files include:

• base.yml: molecule generation using refine-based sampling strategy (default)
• ar.yml: molecule generation using an auto-regressive-like sampling strategy
• simple.yml: molecule generation with only one generation round, not using confidence scores for sampling

Fragment linking

Design molecules by linking fragments for the 416 pairs of proteins and fragments in the fragment linking test set.

python scripts/sample_drug3d.py \
    --config_task configs/sample/test/linking_moad/known_connect.yml \
    --outdir outputs_test/linking_moad \
    --device cuda:0

The task configuration files are in configs/sample/test/linking_moad. Configuration files include:

• known_connect.yml: fragment linking with known connecting atoms of fragments
• unknown_connect.yml: fragment linking with unknown connecting atoms of fragments

PROTAC design

Design PROTAC molecules by linking fragments for the 43 fragment pairs in the PROTAC-DB test set.

python scripts/sample_drug3d.py \
    --config_task configs/sample/test/linking_protacdb/fixed_fragpos.yml \
    --outdir outputs_test/linking_protacdb \
    --device cuda:0

The task configuration files are in configs/sample/test/linking_protacdb. Configuration files include (all assume known connecting atoms of fragments):

• fixed_fragpos.yml: fragment linking with fixed fragment poses
• unfixed_lv0.yml- unfixed_lv4.yml: fragment linking with unfixed fragment poses. The input fragment poses were derived by randomly perturb the true fragment poses with different levels of noise (lv0=smallest).

Fragment growing

Design molecules through growing fragments for the 53 pairs of fragment and protein in the fragment growing test set.

python scripts/sample_drug3d.py \
    --config_task configs/sample/test/growing_csd/base.yml \
    --outdir outputs_test/growing_csd \
    --device cuda:0

The task configuration file is configs/sample/test/growing_csd/base.yml.

De novo peptide design

Design peptides for the 35 protein pockets in the peptide design test set.

python scripts/sample_pdb.py \
    --config_task configs/sample/test/pepdesign_pepbdb/base.yml \
    --outdir outputs_test/pepdesign_pepbdb \
    --device cuda:0

The task configuration file is configs/sample/test/pepdesign_pepbdb/base.yml.

Peptide inverse folding

Design peptides for the 35 pairs of backbone structures and protein pockets in the peptide design test set.

python scripts/sample_pdb.py \
    --config_task configs/sample/test/pepinv_pepbdb/base.yml \
    --outdir outputs_test/pepinv_pepbdb \
    --device cuda:0

The task configuration file is configs/sample/test/pepinv_pepbdb/base.yml.

Sample for provided data

Here, we demonstrate some examples of sampling using the provided data in the data/examples directory.

Run the following command:

python scripts/sample_use.py \
    --config_task configs/sample/examples/dockmol.yml \
    --outdir outputs_examples \
    --device cuda:0

The configuration files are in configs/sample/examples, including:

• Docking
  • dock_smallmol.yml: dock a small molecule to a protein pocket
  • dock_smallmol_flex.yml: dock a small molecule to a protein pocket using flexible noise
  • dock_smallmol_84663.yml: dock the molecule 84663 to caspase-9
  • dock_pep.yml: dock a peptide to a protein pocket
  • dock_pep_fix_some.yml: dock, with fixed coordinates of some atoms
  • dock_pep_know_some.yml: dock, with constrained coordinates of some atoms
• Small molecule design
  • sbdd.yml: design drug-like molecules for protein pocket
  • growing_unfixed_frag.yml: fragment growing with unfixed fragment pose, i.e., design small molecules containing a specified fragment graph for protein pocket
  • growing_fixed_frag.yml: fragment growing with fixed fragment pose, i.e., design small molecules containing a specified fragment with fixed pose for protein pocket
• Peptide design
  • pepdesign.yml: design peptides for protein pocket
• Design with customized settings:
  • pepdesign_hot136E: this directory considers a specific peptide design case. Based on the PD1-PDL1 complex (PDB ID: 3BIK), we found a hot spot residue 136E on PD1 interacting with PDL1. We aim to design a PDL1-binding peptide considering this interaction. We extract the protein fragment around 136E as the input peptide and the PDL1 chain as the target (in data/examples/hot136E). There are several strategies for designing peptdes (see Customized setting explanation for configuration explanation):
    • fixed_Glu_CCOOH: design peptide whose 6th residue (count from 1) is Glu and its -CCOOH group pose is fixed as input.
    • fixed_CCOOH: the designed peptide contains a -CCOOH group and its pose is fixed as input. But the -CCOOH may not be at the 6th residue and may not be in Glu (Asp can also contain -CCOOH).
    • fixed_CCOOH_init0.9: the setting is the same as fixed_CCOOH, but the initial noisy peptide is generated by adding noise to the peptide of the input file, instead of being sampled from the noise prior. The only difference is the parameter noise/init_step. Hint: by setting noise/init_step$< 1$, the initial noisy coordinates will be sampled from the Gaussian noise with mean equal to the input coordinates instead of the noise space center.
    • unfixed_Glu: design peptides with Glu at the 6th residue. No atom coordinates are fixed.
    • unfixed_CCOOH: design peptides containing -CCOOH group (i.e., containing Glu or Asp), but the -CCOOH group can be at any residue index. No atom coordinates are fixed.
    • unfixed_CCOOH_from_inputs: the setting is the same as unfixed_CCOOH, but the initial pose of the -CCOOH group are sampled based on the input peptide. This align with our intuition that the -CCOOH group in the designed peptide should interact with the protein in a similar way as the input one.

More examples are on the way.

Basic configuration explanation

You can refer to these configuration files and adapt to your own data and tasks. Here are some simple explanations of the configuration.

Typically there are five main blocks: sample, data, transforms, task, and noise. The first three keys define the data and sampling parameters, and the last two define the task. In most cases, you only need to find a task template configuration file and modify the first three blocks.

• sample: the sampling parameters, including base random seed, batch size, and the number of generated molecules. The parameter save_traj_prob means the frequency of saving the generation trajectories.
• data: the input data, including
  • protein_path: the path to the protein PDB file.
  • input_ligand: the information of input ligand.
    • For small molecule, it can be a SDF file path, the SMILES string or None (for de novo small mol design).
    • For peptide, it can be the PDB file path, the sequence string (with prefix pep_seq_, e.g., pepseq_DTVFALFW, for docking) or the sequence length (with prefix peplen_, e.g., peplen_10, for de novo design).
  • is_pep: bool, whether the ligand is peptide. It is used to create the PDB files for the generated molecules. If not set, it will be automatically determined according to input_ligand.
  • pocket_args: dict of pocket parameters, including
    • ref_ligand_path: path to the reference molecule file (SDF or PDB). This molecule is used to determine the pocket from the complete protein, i.e., the residues within a certain distance to the reference molecule are defined as pocket residues. Exclusive to pocket_coord.
    • pocket_coord: the coordinate of the pocket. The pocket will be defined as the residues near the coordinate. Exclusive to ref_ligand_path. If neither ref_ligand_path nor pocket_coord is set, it will use input_ligand as reference.
    • radius: the residues within the radius to the reference ligand or the pocket coordinate are defined as pocket residues. Default is 10.
    • criterion: the criterion to define the residue distance, be one of ['center_of_mass', 'min']. Default is 'center_of_mass'.
  • pocmol_args: user-defined identifiers. Not important.
    • data_id
    • pdbid
• transforms
  • featurizer_pocket:
    • center: coordinate space center for denoising. It influences sampling atom coordinates from the Gaussian noise at the first step. If not set, it will be automatically defined as the average of pocket atom coordinates. (You can also use featurizer/mol_as_pocket_center to specify the pocket center)
  • featurizer
    • mol_as_pocket_center: bool, use the center coordinates of the ligand as the space center. If set to True, the parameter data/pocket_args/input_ligand should be SDF/PDB file. (You can also use featurizer_pocket/center to specify the pocket center)
  • variable_mol_size: distributions of the number of atoms for small-molecule designing tasks.
  • variable_sc_size: distributions of number of side-chain atoms for peptide designing. The default value should work well.
• task: the task and its specific mode.
• noise: the task nosie parameters.

Customized setting explanation

Here we explain the customized settings in the examples/pepdesign_hot136E directory.

In these settings, we defined a task called custom. (Basically, all the previous common tasks can be expressed through this custom task.) The basic idea is to (1) define several groups of noise, (2) partition the molecules into several parts, and (3) map the noise groups to the molecule parts.

In their config files, the sample and data blocks are the same as the common tasks. For other blocks:

• transforms: similar as the common tasks, but with some additional settings:
  • The variable_sc_size/applicable_tasks should contain the task name custom.
  • Some side-chain atoms of input peptides will be randomly removed for variable sizes. Set variable_sc_size/not_remove to exclude side-chain atoms from being removed. This is a list of atom indices in the input peptide (starting from 0).
• task: In task/transform, please define:
  • is_peptide: wheter the task is related to peptide or small molecule. This is the prompt $\mathbf{P}^{\text{pep}}$ in the paper.
  • partition: this is where you define how you partition the molecule. It is a list of dictionaries, and each dictionary contains:
    • name: the name of the part.
    • nodes: the atom indices of the part. The atom indices are 0-based.
  • fixed: define which variables are fixed as input, including:
    • node: list of molecular parts whose atom types are fixed.
    • pos: list of molecular parts whose atom coordinates are fixed.
    • edge: list of molecular part pairs whose inner bond types are fixed.
• noise:
  • num_steps: the number of sampling steps. It is an integer and $100$ should work well.
  • init_step: the initial step of noise. It is a scalar in $(0, 1]$ and default is $1$. During the sampling, the step will decay from init_step to $0$ linearly. Larger value means more noise. If it is set as $1$, the initial noisy molecule will be sampled from the noise prior without considering the input molecules. Specifically, the coordinates will be sampled from the Gaussian noise with mean equal to the noise space center. If it is less than $1$ (and the parameter from_prior in the noise group is not set as False (default)), the initial noisy coordinates will be sampled from the Gaussian noise with mean equal to the input coordinates instead of the noise space center.
  • prior: define the noise prior distributions for different noise groups. This is a dictionary, and each key is the noise group name and the value is the noise prior distribution. Tips:
    • For each noise group, define the noise prior distributions for node (atom type), pos (atom coordinate), and edge (bond type). You can refer to the noise prior settings in the training configuration file (configs/train/train_pxm_reduced.yml) for reference.
    • If there is only pos noise, you can set pos_only as True.
    • Set from_prior as True (default) to sample the initial noisy coordinates completely from the noise prior. If you want to consider the input coordinates, you can set from_prior as False to disable the initial noisy coordinates sampling from the noise prior but based on the input coordinates (see unfixed_CCOOH_from_inputs.yml) even if noise/init_step is set as $1$. This is useful when some atom coordinates of the input molecule can provide a good starting point for the generation or their approximate coordinates are known.
  • level: define information level strategies for different noise group. Information level strategy controls the noise scale at each step, i.e., it is a mapping from the step to the information level (within the interval $[0,1]$, information level is $1-$ noise level). Tips:
    • You can refere to the level settings in the training configuration file (configs/train/train_pxm_reduced.yml) for reference.
    • Usually the uniform level should work well for de novo generation. If you want to preserve more information of the input file, you can set the min level as a larger value.
  • mapper: define the mapping from the noise groups to the molecule parts. This is a dictionary, and each key is the noise group name and the value is the molecule part name of the variables node (atom type), pos (atom coordinate), and edge (bond type).

Train

Make sure to download and extract the training data data_training_processed_reduced.tar.gz as described in the Data and model weights section. Then run the following command to train the model with reduced data:

python scripts/train_pl.py --config configs/train/train_pxm_reduced.yml --num_gpus 1

You can specify the number of GPUs to use by setting the num_gpus parameter. The training configuration file is defined in configs/train/train_pxm_reduced.yml. You can change the batch_size parameter in the configuration file to adjust to your GPU memory.

If you want to train the model with the full training data, please follow the instructions in the Raw data and processing steps section to process the raw data for training. Then, modify data.dataset.root and data.dataset.assembly_path in the training configuration file to point to the full training data directory and run the training command as above.