Awesome
MolCRAFT
Official implementation of ICML 2024 "MolCRAFT: Structure-Based Drug Design in Continuous Parameter Space".
🎉 Our demo is now available at 120.240.170.153:10990. The formal version will be at http://gensi-thuair.com:10990/ soon. Welcome to have a try!
Environment
It is highly recommended to install via docker if a Linux server with NVIDIA GPU is available.
Otherwise, you might check README for env for further details of docker or conda setup.
Prerequisite
A docker with nvidia-container-runtime
enabled on your Linux system is required.
[!TIP]
- This repo provides an easy-to-use script to install docker and nvidia-container-runtime, in
./docker
runsudo ./setup_docker_for_host.sh
to set up your host machine.- For details, please refer to the install guide.
Install via Docker
We highly recommend you to set up the environment via docker, since all you need to do is a simple make
command.
cd ./docker
make
Data
Data used for training / evaluating the model should be put in the data
folder by default, and accessible in the data Google Drive folder.
To train the model from scratch, download the lmdb file and split file into data folder:
crossdocked_v1.1_rmsd1.0_pocket10_processed_final.lmdb
crossdocked_pocket10_pose_split.pt
To evaluate the model on the test set, download and unzip the test_set.zip
into data folder. It includes the original PDB files that will be used in Vina Docking.
By default, We transform the lmdb further into the featurized dataset as crossdocked_v1.1_rmsd1.0_pocket10_add_aromatic_transformed_simple.pt
as described in transform.py
, which might take several minutes. To enable accelerated training, the yaml file will be set as follows:
data:
name: pl_tr # [pl, pl_tr] where tr means offline-transformed
Training
Run make -f scripts.mk
(without the need for data preparation), or alternatively (with data folder correctly configured),
python train_bfn.py --exp_name ${EXP_NAME} --revision ${REVISION}
where the default values should be set the same as:
python train_bfn.py --sigma1_coord 0.03 --beta1 1.5 --lr 5e-4 --time_emb_dim 1 --epochs 15 --max_grad_norm Q --destination_prediction True --use_discrete_t True --num_samples 10 --sampling_strategy end_back_pmf
Testing
For quick evaluation of the official checkpoint, refer to make evaluate
in scripts.mk
:
python train_bfn.py --test_only --no_wandb --ckpt_path ./checkpoints/last.ckpt
Debugging
For quick debugging training process, run make debug -f scripts.mk
:
python train_bfn.py --no_wandb --debug --epochs 1
Sampling
We provide the pretrained checkpoint as last.ckpt.
Sampling for pockets in the testset
Run make evaluate -f scripts.mk
, or alternatively,
python train_bfn.py --config_file configs/default.yaml --exp_name ${EXP_NAME} --revision ${REVISION} --test_only --num_samples ${NUM_MOLS_PER_POCKET} --sample_steps 100
The output molecules vina_docked.pt
for all 100 test pockets will be saved in ./logs/${USER}_bfn_sbdd/${EXP_NAME}/${REVISION}/test_outputs/${TIMESTAMP}
folders.
Sampling from pdb file
To sample from a whole protein pdb file, we need the corresponding reference ligand to clip the protein pocket (a 10A region around the reference position).
Below is an example that stores the generated 10 molecules under output
folder. The configurations are managed in the call()
function of sample_for_pocket.py
.
python sample_for_pocket.py ${PDB_PATH} ${SDF_PATH}
Evaluation
Evaluating molecules
For binding affinity (Vina Score / Min / Dock) and molecular properties (QED, SA), it is calculated upon sampling.
For PoseCheck (strain energy, clashes) and other conformational results (bond length, bond angle, torsion angle, RMSD), please refer to test
folder.
Evaluating meta files
We provide samples for all SBDD baselines in the sample Google Drive folder.
You may download the all_samples.tar.gz
and then tar xzvf all_samples.tar.gz
, which extracts all the pt files into samples
folder for evaluation.
Citation
@article{qu2024molcraft,
title={MolCRAFT: Structure-Based Drug Design in Continuous Parameter Space},
author={Qu, Yanru and Qiu, Keyue and Song, Yuxuan and Gong, Jingjing and Han, Jiawei and Zheng, Mingyue and Zhou, Hao and Ma, Wei-Ying},
journal={ICML 2024},
year={2024}
}
@article{song2024unified,
title={Unified Generative Modeling of 3D Molecules via Bayesian Flow Networks},
author={Song, Yuxuan and Gong, Jingjing and Qu, Yanru and Zhou, Hao and Zheng, Mingyue and Liu, Jingjing and Ma, Wei-Ying},
journal={ICLR 2024},
year={2024}
}