Source code for torchdrug.datasets.bindingdb

import os

from rdkit import Chem

from torch.utils import data as torch_data

from torchdrug import data, utils
from torchdrug.core import Registry as R


[docs]@R.register("datasets.BindingDB") @utils.copy_args(data.ProteinLigandDataset.load_lmdbs, ignore=("sequence_field", "smiles_field", "target_fields")) class BindingDB(data.ProteinLigandDataset): """ The BindingDB dataset with binding affinity indicating the interaction strength between pairs of protein and ligand. Statistics: - #Train: 7,900 - #Valid: 878 - #Test: 5,230 Parameters: path (str): the path to store the dataset verbose (int, optional): output verbose level **kwargs """ url = "https://miladeepgraphlearningproteindata.s3.us-east-2.amazonaws.com/peerdata/BindingDB_Kd.tar.gz" md5 = "0b207cb962c4945f9003fc020b415a74" splits = ["train", "valid", "random_test", "holdout_test"] target_fields = ["affinity"] def __init__(self, path, verbose=1, **kwargs): path = os.path.expanduser(path) if not os.path.exists(path): os.makedirs(path) self.path = path zip_file = utils.download(self.url, path, md5=self.md5) data_path = utils.extract(zip_file) lmdb_files = [os.path.join(data_path, "BindingDB_Kd_%s.lmdb" % split) for split in self.splits] self.load_lmdbs(lmdb_files, sequence_field="target", smiles_field="drug", target_fields=self.target_fields, verbose=verbose, **kwargs) def split(self, keys=None): keys = keys or self.splits offset = 0 splits = [] for split_name, num_sample in zip(self.splits, self.num_samples): if split_name in keys: split = torch_data.Subset(self, range(offset, offset + num_sample)) splits.append(split) offset += num_sample return splits def get_item(self, index): if self.lazy: graph1 = data.Protein.from_sequence(self.sequences[index], **self.kwargs) mol = Chem.MolFromSmiles(self.smiles[index]) if not mol: graph2 = None else: graph2 = data.Molecule.from_molecule(mol, **self.kwargs) else: graph1 = self.data[index][0] graph2 = self.data[index][1] item = {"graph1": graph1, "graph2": graph2} item.update({k: v[index] for k, v in self.targets.items()}) if self.transform: item = self.transform(item) return item