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An all-atom protein generative model

delete2024-06-25
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OA
AI
A
Alexander E. Chu
J
Jinho Kim
L
Lucy Cheng
G
Gina El Nesr
M
Minkai Xu
R
Richard W. Shuai
P
Po‐Ssu Huang *
DOI:10.1073/pnas.2311500121delete
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Abstract

Abstract

En 中文
Proteins mediate their functions through chemical interactions; modeling these interactions, which are typically through sidechains, is an important need in protein design. However, constructing an all-atom generative model requires an appropriate scheme for managing the jointly continuous and discrete nature of proteins encoded in the structure and sequence. We describe an all-atom diffusion model of protein structure, Protpardelle, which represents all sidechain states at once as a superposition state; superpositions defining a protein are collapsed into individual residue types and conformations during sample generation. When combined with sequence design methods, our model is able to codesign all-atom protein structure and sequence. Generated proteins are of good quality under the typical quality, diversity, and novelty metrics, and sidechains reproduce the chemical features and behavior of natural proteins. Finally, we explore the potential of our model to conduct all-atom protein design and scaffold functional motifs in a backbone- and rotamer-free way.
Keywords:
protein design | protein structure | generative modeling | sidechain generation | full -atom model
engineering. Generative modeling
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Journal

P
Proceedings of the National Academy of Sciences of the United States of America
IF:
9.1
Papers:
10.8W
Citations:
73.5W

Organization

S
Stanford University
Scholars:
9.6W
Papers: 8.2W
Citations: 17.0W
G
Google Incorporated
Scholars:
3.5K
Papers: 1.8K
Citations: 8