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DiffDock-PP: Rigid Protein-Protein Docking with Diffusion Models

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arxiv 2304.03889 v1 pith:W5266PH7 submitted 2023-04-08 q-bio.BM cs.LG

classification q-bio.BMcs.LG
keywords diffdock-ppdockingbaselinesdiffusiongenerativelearningmethodsperformance
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abstract

Understanding how proteins structurally interact is crucial to modern biology, with applications in drug discovery and protein design. Recent machine learning methods have formulated protein-small molecule docking as a generative problem with significant performance boosts over both traditional and deep learning baselines. In this work, we propose a similar approach for rigid protein-protein docking: DiffDock-PP is a diffusion generative model that learns to translate and rotate unbound protein structures into their bound conformations. We achieve state-of-the-art performance on DIPS with a median C-RMSD of 4.85, outperforming all considered baselines. Additionally, DiffDock-PP is faster than all search-based methods and generates reliable confidence estimates for its predictions. Our code is publicly available at $\texttt{https://github.com/ketatam/DiffDock-PP}$

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Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. From thermodynamics to protein design: Diffusion models for biomolecule generation towards autonomous protein engineering

    q-bio.QM 2025-01 conditional novelty 3.0 of 10

    A survey of diffusion models for biomolecule generation, organized around DDPM and score-based frameworks, equivariance, 56 application models, benchmarks, and future directions for autonomous protein engineering.

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