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Data-Efficient Protein 3D Geometric Pretraining via Refinement of Diffused Protein Structure Decoy

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arxiv 2302.10888 v1 pith:BHIPTV42 submitted 2023-02-05 cs.LG cs.AIq-bio.BM

classification cs.LGcs.AIq-bio.BM
keywords proteinpretrainingstructuretaskschallengesdatadata-efficientdecoy
verification ladder T0 review T1 audit T2 compute T3 formal
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Learning meaningful protein representation is important for a variety of biological downstream tasks such as structure-based drug design. Having witnessed the success of protein sequence pretraining, pretraining for structural data which is more informative has become a promising research topic. However, there are three major challenges facing protein structure pretraining: insufficient sample diversity, physically unrealistic modeling, and the lack of protein-specific pretext tasks. To try to address these challenges, we present the 3D Geometric Pretraining. In this paper, we propose a unified framework for protein pretraining and a 3D geometric-based, data-efficient, and protein-specific pretext task: RefineDiff (Refine the Diffused Protein Structure Decoy). After pretraining our geometric-aware model with this task on limited data(less than 1% of SOTA models), we obtained informative protein representations that can achieve comparable performance for various downstream tasks.

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Cited by 2 Pith papers

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

  1. DapPep: Domain Adaptive Peptide-agnostic Learning for Universal T-cell Receptor-antigen Binding Affinity Prediction

    q-bio.QM 2024-11 conditional novelty 5.0 of 10

    DapPep, built from ESM-2 with cross-attention and peptide-reconstruction pre-training, reports ROC-AUC 0.816 and PR-AUC 0.836 on unseen peptides, beating PanPep by about 9 to 11 percent.

  2. Pan-protein Design Learning Enables Task-adaptive Generalization for Low-resource Enzyme Design

    q-bio.QM 2024-11 conditional novelty 5.0 of 10

    CrossDesign aligns pretrained protein language models with structure encoders to improve enzyme sequence design and zero-shot mutation fitness prediction.

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