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9FSA

Cell wall anchoring domain of the surface layer protein of Methanococcus voltae (aa 24-75; 484-576)

9FSA の概要
エントリーDOI10.2210/pdb9fsa/pdb
分子名称S-layer protein (2 entities in total)
機能のキーワードsurface layer protein, self assembly, cell wall binding, anchoring, symmetry, structural protein
由来する生物種Methanococcus voltae
詳細
タンパク質・核酸の鎖数1
化学式量合計15757.84
構造登録者
Grininger, C.,Sagmeister, T.,Pavkov-Keller, T. (登録日: 2024-06-20, 公開日: 2024-08-28, 最終更新日: 2024-10-02)
主引用文献Buhlheller, C.,Sagmeister, T.,Grininger, C.,Gubensak, N.,Sleytr, U.B.,Uson, I.,Pavkov-Keller, T.
SymProFold: Structural prediction of symmetrical biological assemblies.
Nat Commun, 15:8152-8152, 2024
Cited by
PubMed Abstract: Symmetry in nature often emerges from self-assembly processes and serves a wide range of functions. Cell surface layers (S-layers) form symmetrical lattices on many bacterial and archaeal cells, playing essential roles such as facilitating cell adhesion, evading the immune system, and protecting against environmental stress. However, the experimental structural characterization of these S-layers is challenging due to their self-assembly properties and high sequence variability. In this study, we introduce the SymProFold pipeline, which utilizes the high accuracy of AlphaFold-Multimer predictions to derive symmetrical assemblies from protein sequences, specifically focusing on two-dimensional S-layer arrays and spherical viral capsids. The pipeline tests all known symmetry operations observed in these systems (p1, p2, p3, p4, and p6) and identifies the most likely symmetry for the assembly. The predicted models were validated using available experimental data at the cellular level, and additional crystal structures were obtained to confirm the symmetry and interfaces of several SymProFold assemblies. Overall, the SymProFold pipeline enables the determination of symmetric protein assemblies linked to critical functions, thereby opening possibilities for exploring functionalities and designing targeted applications in diverse fields such as nanotechnology, biotechnology, medicine, and materials and environmental sciences.
PubMed: 39294115
DOI: 10.1038/s41467-024-52138-3
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.05 Å)
構造検証レポート
Validation report summary of 9fsa
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-02-04に公開中

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