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Generative De Novo Protein Design with Global Context

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arxiv 2204.10673 v2 pith:MNWEL7LY submitted 2022-04-21 q-bio.BM cs.AIcs.LG

classification q-bio.BMcs.AIcs.LG
keywords proteindesignstructuregloballocalacidsaminomodules
verification ladder T0 review T1 audit T2 compute T3 formal
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The linear sequence of amino acids determines protein structure and function. Protein design, known as the inverse of protein structure prediction, aims to obtain a novel protein sequence that will fold into the defined structure. Recent works on computational protein design have studied designing sequences for the desired backbone structure with local positional information and achieved competitive performance. However, similar local environments in different backbone structures may result in different amino acids, indicating that protein structure's global context matters. Thus, we propose the Global-Context Aware generative de novo protein design method (GCA), consisting of local and global modules. While local modules focus on relationships between neighbor amino acids, global modules explicitly capture non-local contexts. Experimental results demonstrate that the proposed GCA method outperforms state-of-the-arts on de novo protein design. Our code and pretrained model will be released.

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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. ProtInvTree: Deliberate Protein Inverse Folding with Reward-guided Tree Search

    q-bio.BM 2025-06 conditional novelty 6.0 of 10

    A reward-guided tree search over a frozen protein language model designs diverse sequences that score higher on ESMFold-based self-consistency benchmarks than existing inverse folding methods.

  2. EnerBridge-DPO: Energy-Guided Protein Inverse Folding with Markov Bridges and Direct Preference Optimization

    cs.LG 2025-06 conditional novelty 5.0 of 10

    A Markov-bridge inverse folding model fine-tuned with energy-based preference pairs and an explicit ΔΔG loss designs lower-energy protein complex sequences while keeping sequence recovery close to state-of-the-art.

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