ArticleProtein science : a publication of the Protein Society2025
DiffPepDock: Efficient protein-peptide docking and binder screening via SE(3)-equivariant diffusion.
Article in Protein science : a publication of the Protein Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Strategic Template Filtering Accelerates Fragment-Based Peptide Docking.Journal of chemical information and modeling · 2026Article
- Bridging Generative AI and Diffusion Models With Molecular Simulation to Design Anti-Quorum-Sensing De novo Peptides Targeting LasR of Pseudomonas aeruginosa.Probiotics and antimicrobial proteins · 2026Article
- Peptide-protein docking: from physics-based models to generative intelligence.Chemical communications (Cambridge, England) · 2026Review
- A Review of Current Computational Tools for Peptide-Protein Docking.Journal of computational chemistry · 2026Review
- DiffPepDock: Efficient protein-peptide docking and binder screening via SE(3)-equivariant diffusion.Protein science : a publication of the Protein Society · 2025Article
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Authors and funding
5 authors.
Funding
Abstract
Accurate modeling of protein-peptide interactions is critical for elucidating peptide-mediated biological processes and advancing drug discovery. While traditional methods and recent deep learning-based approaches have shown promise, they often face limitations in accuracy, generalizability, computational efficiency, and the integration of prior binding knowledge. Here, we present DiffPepDock, an efficient protein-peptide docking tool based on SE(3)-equivariant diffusion models. DiffPepDock is pretrained on a carefully curated synthetic dataset of protein-fragment complexes and subsequently fine-tuned on high-quality experimental protein-peptide structures, combining generalization capability with task-specific accuracy. It also supports incorporation of user-specified binding priors including known binding motifs or reference ligands to facilitate pocket selection and enhance docking accuracy. Benchmarking on a non-redundant time-split test set demonstrates that DiffPepDock achieves accuracy comparable to state-of-the-art methods such as AlphaFold3, while substantially reducing inference time. Case studies further underscore its capability in accurately reconstructing native binding structures, particularly in scenarios where AlphaFold3 exhibits limitations. Moreover, DiffPepDock shows competitive in silico screening performance for identifying true peptide binders on AlphaFold-predicted targets, underscoring its practical utility in real-world applications. We anticipate that DiffPepDock offers a practical and reliable tool for protein-peptide docking, complementing existing biomolecular structure prediction methods and contributing to peptide therapeutic modeling efforts. The DiffPepDock tool is publicly available at https://github.com/YuzheWangPKU/DiffPepBuilder, with an interactive demonstration provided via Google Colab at https://colab.research.google.com/github/YuzheWangPKU/DiffPepBuilder/blob/main/examples/DiffPepDock_demo.ipynb.
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Registered trials
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