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5KPE

Solution NMR Structure of Denovo Beta Sheet Design Protein, Northeast Structural Genomics Consortium (NESG) Target OR664

5KPE の概要
エントリーDOI10.2210/pdb5kpe/pdb
関連するPDBエントリー5KPH
NMR情報BMRB: 30128
分子名称De novo Beta Sheet Design Protein OR664 (1 entity in total)
機能のキーワードstructural genomics, psi-biology, northeast structural genomics consortium, nesg, de novo protein
由来する生物種synthetic construct
タンパク質・核酸の鎖数1
化学式量合計13594.00
構造登録者
Tang, Y.,Liu, G.,Baker, D.,Montelione, G.T.,Northeast Structural Genomics Consortium (NESG) (登録日: 2016-07-03, 公開日: 2016-09-21, 最終更新日: 2024-05-15)
主引用文献Marcos, E.,Basanta, B.,Chidyausiku, T.M.,Tang, Y.,Oberdorfer, G.,Liu, G.,Swapna, G.V.,Guan, R.,Silva, D.A.,Dou, J.,Pereira, J.H.,Xiao, R.,Sankaran, B.,Zwart, P.H.,Montelione, G.T.,Baker, D.
Principles for designing proteins with cavities formed by curved beta sheets.
Science, 355:201-206, 2017
Cited by
PubMed Abstract: Active sites and ligand-binding cavities in native proteins are often formed by curved β sheets, and the ability to control β-sheet curvature would allow design of binding proteins with cavities customized to specific ligands. Toward this end, we investigated the mechanisms controlling β-sheet curvature by studying the geometry of β sheets in naturally occurring protein structures and folding simulations. The principles emerging from this analysis were used to design, de novo, a series of proteins with curved β sheets topped with α helices. Nuclear magnetic resonance and crystal structures of the designs closely match the computational models, showing that β-sheet curvature can be controlled with atomic-level accuracy. Our approach enables the design of proteins with cavities and provides a route to custom design ligand-binding and catalytic sites.
PubMed: 28082595
DOI: 10.1126/science.aah7389
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 5kpe
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2025-06-25に公開中

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