The results indicate that frozen multi-view graph representations, explicit physicochemical statistics, and heterogeneous model fusion provide a robust and flexible framework for protein-ligand binding-affinity prediction.
Abstract
Quantitative estimation of protein-ligand binding affinity from three-dimensional complex structures is a fundamental task in structure-based computational chemistry and molecular modeling. Reliable prediction remains challenging because available structure-affinity data are limited, experimentally heterogeneous, conformation-dependent, and sensitive to dataset partitioning. RAVEN (Randomized Atomistic Views with Ensemble Neural Reservoirs) utilizes a multihead reservoir of independently initialized and fully frozen atomistic graph encoders to generate diverse structural projections without end-to-end optimization of the graph representation. These projections are integrated with a deterministic physicochemical interaction fingerprint and processed by heterogeneous supervised readers, including neural and tree-based regressors, whose outputs are combined through validation-based nonnegative fusion. The random reservoir expands structural feature coverage across independent encoder realizations, whereas the explicit physicochemical descriptors and heterogeneous readers contribute complementary information and distinct inductive biases. Evaluation on a similarity-isolated PDBbind 2020R1 split reconstructed using GEMS similarity resources, together with the protected CASF-2016 subset, demonstrated strong predictive performance. The results indicate that frozen multi-view graph representations, explicit physicochemical statistics, and heterogeneous model fusion provide a robust and flexible framework for protein-ligand binding-affinity prediction.
Predicting ligand binding sites on protein surfaces requires capturing complex local geometries and satisfying physical constraints. Existing voxel-based methods suffer from high computational costs and rotation sensitivity, while standard point-cloud GNNs often lack geometric completeness—failing to distinguish chiral...
Kang-Xin Chen, Jie-Yu Zhao, Jin-Li Hu et al.· Proceedings of the Thirty-Fi...· 0 citations
An Algebraic Graph Neural Network model designed to encode molecular structures into a low-dimensional graph representation while preserving critical biochemical interactions is introduced, demonstrating superior performance in binding affinity prediction compared to state-of-the-art scoring functions.
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By combining protein language model embeddings with topology-adaptive geometric reasoning, DiConSite offers a reusable framework for residue-level protein interaction analysis and achieves consistently strong and often best-performing results, while improving robustness to structural uncertainty and cross-modal variati...
Shou-Zhi Chen, Zhen-Chao Tang, Lin-Lin You et al.· IEEE Transactions on Pattern...· 1 citation
Abstract Motivation To enable real-world protein-ligand affinity prediction, not only out-of-distribution generalization but also robustness to variable structural availability and quality should be considered in model design. Results We present AlignNet, a hierarchical representation alignment framework that mitigates...
Xiaowen Hu, Hong-Yi Huang, Hao Sun et al.· Bioinform.· 0 citations
Accurate prediction of drug-target binding affinity (DTA) is a key task in virtual screening. However, current computational methods face a key challenge: sequence-based approaches often fail to capture critical spatial information, while structure-based models rely on computationally expensive 3D coordinates, which re...
Junlin Xu, Ye Yuan, Menglong Hu et al.· IEEE journal of biomedical a...· 0 citations
RGTBind, a graph transformer that combines multi-scale radial basis function distance encoding with a learnable threshold-gating mechanism to model spatially informative residue interactions, achieved the best F1, AUC, and MCC among the compared methods.
Yi Qiu, Duo Zhao, Y. Ye et al.· Journal of Molecular Modelin...· 0 citations
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