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Annotation-guided Protein Design with Multi-Level Domain Alignment

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arxiv 2404.16866 v4 pith:2XTVARP6 submitted 2024-04-18 q-bio.QM cs.AIcs.LG

classification q-bio.QMcs.AIcs.LG
keywords proteindesignannotationspaagproteinsalignmentdomaingeneration
verification ladder T0 review T1 audit T2 compute T3 formal
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The core challenge of de novo protein design lies in creating proteins with specific functions or properties, guided by certain conditions. Current models explore to generate protein using structural and evolutionary guidance, which only provide indirect conditions concerning functions and properties. However, textual annotations of proteins, especially the annotations for protein domains, which directly describe the protein's high-level functionalities, properties, and their correlation with target amino acid sequences, remain unexplored in the context of protein design tasks. In this paper, we propose Protein-Annotation Alignment Generation, PAAG, a multi-modality protein design framework that integrates the textual annotations extracted from protein database for controllable generation in sequence space. Specifically, within a multi-level alignment module, PAAG can explicitly generate proteins containing specific domains conditioned on the corresponding domain annotations, and can even design novel proteins with flexible combinations of different kinds of annotations. Our experimental results underscore the superiority of the aligned protein representations from PAAG over 7 prediction tasks. Furthermore, PAAG demonstrates a significant increase in generation success rate (24.7% vs 4.7% in zinc finger, and 54.3% vs 22.0% in the immunoglobulin domain) in comparison to the existing model. We anticipate that PAAG will broaden the horizons of protein design by leveraging the knowledge from between textual annotation and proteins.

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Cited by 1 Pith paper

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  1. PDFBench: A Benchmark for De novo Protein Design from Function

    cs.LG 2025-05 conditional novelty 6.0 of 10

    The paper presents PDFBench, a unified benchmark with 16 metrics and a new post-2025 protein test set, and finds that evaluation choices such as retrieval strategy or supported keywords can dominate model rankings.

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