Evidence map›Paper›PMID 41088767›Full record

ArticleProtein science : a publication of the Protein Society2025

DiffPepDock: Efficient protein-peptide docking and binder screening via SE(3)-equivariant diffusion.

Yuzhe Wang, Fanhao Wang, Laiyi Feng, Changsheng Zhang, Luhua Lai

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Strategic Template Filtering Accelerates Fragment-Based Peptide Docking.Journal of chemical information and modeling · 2026
    Article
  2. Article
  3. Peptide-protein docking: from physics-based models to generative intelligence.Chemical communications (Cambridge, England) · 2026
    Review
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yuzhe WangCenter for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.ORCID 0009-0007-3680-0308
Fanhao WangCenter for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Laiyi FengCenter for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Changsheng ZhangBNLMS, College of Chemistry and Molecular Engineering, Peking University, Beijing, China.
Luhua LaiCenter for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.ORCID 0000-0002-8343-7587

Funding

Chinese Academy of Medical Sciences 2021- I2M-5-014National Key Research and Development Program of China 2022YFA1303700National Natural Science Foundation of China 21977007National Natural Science Foundation of China T2321001
6 · The paper itself

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.

Indexed as

Molecular Docking SimulationPeptidesProteinsSoftwareBinding SitesLigandsProtein BindingLigandsPeptidesProteinsDiffPepDockdiffusion modelsprotein–peptide docking

Identifiers

PMID41088767
PMCPMC12521636

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.