反向
折叠(DSP实现)
计算机科学
蛋白质折叠
物理
数学
工程类
几何学
电气工程
核磁共振
作者
Shugao Chen,Ziyao Li,Xiangxiang Zeng,Guolin Ke
标识
DOI:10.1101/2023.11.07.565939
摘要
Abstract Recent advances in deep learning enable new approaches to protein design through inverse folding and backbone generation. However, backbone generators may produce structures that inverse folding struggles to identify sequences for, indicating designability issues. We propose Amalga, an inference-time technique that enhances designability of backbone generators. Amalga leverages folding and inverse folding models to guide backbone generation towards more designable conformations by incorporating “folded-from-inverse-folded” (FIF) structures. To generate FIF structures, possible sequences are predicted from step-wise predictions in the reverse diffusion and further folded into new backbones. Being intrinsically designable, the FIF structures guide the generated backbones to a more designable distribution. Experiments on both de novo design and motif-scaffolding demonstrate improved designability and diversity with Amalga on RFdiffusion.
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