Combining docking pose rank and structure with deep learning improves protein-ligand binding mode prediction
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Abstract (arXiv)
We present a simple, modular graph-based convolutional neural network that takes structural information from protein-ligand complexes as input to generate models for activity and binding mode prediction. Complex structures are generated by a standard docking procedure and fed into a dual-graph architecture that includes separate sub-networks for the ligand bonded topology and the ligand-protein contact map. This network division allows contributions from ligand identity to be distinguished from effects of protein-ligand interactions on classification. We show, in agreement with recent literature, that dataset bias drives many of the promising results on virtual screening that have previously been reported. However, we also show that our neural network is capable of learning from protein structural information when, as in the case of binding mode prediction, an unbiased dataset is constructed. We develop a deep learning model for binding mode prediction that uses docking ranking as input in combination with docking structures. This strategy mirrors past consensus models and outperforms the baseline docking program in a variety of tests, including on cross-docking datasets that mimic real-world docking use cases. Furthermore, the magnitudes of network predictions serve as reliable measures of model confidence
Key facts. Cited by 10 papers in the map (data through 7 Oct 2026). First posted on arXiv 7 Oct 2019.
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Citing papers per year: 2021: 2; 2022: 4; 2023: 2; 2024: 2.
10 papers.
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- 2021Assigning Confidence to Molecular Property Predictioncited by 14
- 2022Structure-based drug discovery with deep learningcited by 3
- 2021Analysis of training and seed bias in small molecules generated with a conditional graph-based variational autoencoder -- Insights for practical AI-driven molecule generationcited by 1
- 2023FlexVDW: A machine learning approach to account for protein flexibility in ligand dockingcited by 1
- 2024Multi-view biomedical foundation models for molecule-target and property predictioncited by 1
- 2022Recent Developments in Structure-Based Virtual Screening Approachescited by 0
- 2023Transferable Graph Neural Fingerprint Models for Quick Response to Future Bio-Threatscited by 0
- 2024Multi-view biomedical foundation models for molecule-target and property prediction25 Oct 2024
- 2024Tx-LLM: A Large Language Model for Therapeutics10 Jun 2024
- 2023Transferable Graph Neural Fingerprint Models for Quick Response to Future Bio-Threats17 Jul 2023
- 2023FlexVDW: A machine learning approach to account for protein flexibility in ligand docking20 Mar 2023
- 2022Structure-based drug discovery with deep learning26 Dec 2022
- 2022Recent Developments in Structure-Based Virtual Screening Approaches6 Nov 2022
- 2022Graph Neural Networks for Molecules12 Sep 2022
- 2022EquiBind: Geometric Deep Learning for Drug Binding Structure Prediction7 Feb 2022
- 2021Analysis of training and seed bias in small molecules generated with a conditional graph-based variational autoencoder -- Insights for practical AI-driven molecule generation19 Jul 2021
- 2021Assigning Confidence to Molecular Property Prediction23 Feb 2021