Interpretable Chirality-Aware Graph Neural Network forQuantitative Structure Activity Relationship Modeling in Drug Discovery
Liu, Y.; Wang, Y.; Vu, O. T.; Moretti, R.; Bodenheimer, B.; Meiler, J.; Derr, T.
Show abstract
In computer-aided drug discovery, quantitative structure activity relation models are trained to predict biological activity from chemical structure. Despite the recent success of applying graph neural network to this task, important chemical information such as molecular chirality is ignored. To fill this crucial gap, we propose Molecular-Kernel Graph Neural Network (MolKGNN) for molecular representation learning, which features SE(3)-/conformation invariance, chiralityawareness, and interpretability. For our MolKGNN, we first design a molecular graph convolution to capture the chemical pattern by comparing the atoms similarity with the learnable molecular kernels. Furthermore, we propagate the similarity score to capture the higher-order chemical pattern. To assess the method, we conduct a comprehensive evaluation with nine well-curated datasets spanning numerous important drug targets that feature realistic high class imbalance and it demonstrates the superiority of MolKGNN over other GNNs in CADD. Meanwhile, the learned kernels identify patterns that agree with domain knowledge, confirming the pragmatic interpretability of this approach. Our codes are publicly available at https://github.com/meilerlab/MolKGNN.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- GraphDTA: Predicting drug-target binding affinity with graph neural networks 97%
- FL-QSAR: a federated learning based QSAR prototype for collaborative drug discovery 97%
- DTI-Voodoo: machine learning over interaction networks and ontology-based background knowledge predicts drug-target interactions 97%
Similar papers in this journal
- Data Imbalance in Drug Response Prediction - Multi-Objective Optimization Approach in Deep Learning Setting 97%
- GexMolGen: Cross-modal Generation of Hit-like Molecules via Large Language Model Encoding of Gene Expression Signatures 96%
- DeepDDS: deep graph neural network with attention mechanism to predict synergistic drug combinations 96%
Similar papers in this journal
- FLONE: fully Lorentz network embedding for inferring novel drug targets 96%
- A Graph-Attention-Based Deep Learning Network for Predicting Biotech-Small-Molecule Drug Interactions 96%
- Mining drug-target interactions from biomedical literature using chemical and gene descriptions-based ensemble transformer model. 95%
Similar papers in this journal
- Evaluation of network architecture and data augmentation methods for deep learning in chemogenomics 96%
- Chemical Genomics Language Model toward Reliable and Explainable Compound-Protein Interaction Exploration 96%
- DeepGraphMol, a multi-objective, computational strategy for generating molecules with desirable properties: a graph convolution and reinforcement learning approach 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.