Refold: Refining Protein Inverse Folding with Efficient Structural Matching and Fusion
Yiran Zhu, Changxi Chi, Hongxin Xiang, Wenjie Du, Xiaoqi Wang, Jun Xia

TL;DR
Refold is a new framework that combines database-derived structural priors with deep learning to improve protein inverse folding, achieving state-of-the-art accuracy and better handling of uncertain regions.
Contribution
Refold introduces a synergistic method that integrates structural priors with deep learning predictions, including a Dynamic Utility Gate to manage prior quality, advancing protein inverse folding.
Findings
Achieves 0.63 native sequence recovery on benchmarks.
Delivers larger improvements in high-uncertainty regions.
Outperforms existing methods in standard evaluations.
Abstract
Protein inverse folding aims to design an amino acid sequence that will fold into a given backbone structure, serving as a central task in protein design. Two main paradigms have been widely explored. Template-based methods exploit database-derived structural priors and can achieve high local precision when close structural neighbors are available, but their dependence on database coverage and match quality often degrades performance on out-of-distribution (OOD) targets. Deep learning approaches, in contrast, learn general structure-to-sequence regularities and usually generalize better to new backbones. However, they struggle to capture fine-grained local structure, which can cause uncertain residue predictions and missed local motifs in ambiguous regions. We introduce Refold, a novel framework that synergistically integrates the strengths of database-derived structural priors and deep…
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Taxonomy
TopicsProtein Structure and Dynamics · Enzyme Structure and Function · Machine Learning in Materials Science
