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6GBK

Repertoires of functionally diverse enzymes through computational design at epistatic active-site positions

6GBK の概要
エントリーDOI10.2210/pdb6gbk/pdb
分子名称Parathion hydrolase, FORMIC ACID, ZINC ION, ... (5 entities in total)
機能のキーワードphosphotriesterase, hydrolase
由来する生物種Brevundimonas diminuta (Pseudomonas diminuta)
タンパク質・核酸の鎖数2
化学式量合計73408.05
構造登録者
Khersonsky, O.,Lipsh, R.,Avizemer, Z.,Goldsmith, M.,Ashani, Y.,Leader, H.,Dym, O.,Rogotner, S.,Trudeau, D.,Tawfik, D.S.,Fleishman, S.J. (登録日: 2018-04-15, 公開日: 2018-10-24, 最終更新日: 2024-01-17)
主引用文献Khersonsky, O.,Lipsh, R.,Avizemer, Z.,Ashani, Y.,Goldsmith, M.,Leader, H.,Dym, O.,Rogotner, S.,Trudeau, D.L.,Prilusky, J.,Amengual-Rigo, P.,Guallar, V.,Tawfik, D.S.,Fleishman, S.J.
Automated Design of Efficient and Functionally Diverse Enzyme Repertoires.
Mol. Cell, 72:178-186.e5, 2018
Cited by
PubMed Abstract: Substantial improvements in enzyme activity demand multiple mutations at spatially proximal positions in the active site. Such mutations, however, often exhibit unpredictable epistatic (non-additive) effects on activity. Here we describe FuncLib, an automated method for designing multipoint mutations at enzyme active sites using phylogenetic analysis and Rosetta design calculations. We applied FuncLib to two unrelated enzymes, a phosphotriesterase and an acetyl-CoA synthetase. All designs were active, and most showed activity profiles that significantly differed from the wild-type and from one another. Several dozen designs with only 3-6 active-site mutations exhibited 10- to 4,000-fold higher efficiencies with a range of alternative substrates, including hydrolysis of the toxic organophosphate nerve agents soman and cyclosarin and synthesis of butyryl-CoA. FuncLib is implemented as a web server (http://FuncLib.weizmann.ac.il); it circumvents iterative, high-throughput experimental screens and opens the way to designing highly efficient and diverse catalytic repertoires.
PubMed: 30270109
DOI: 10.1016/j.molcel.2018.08.033
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 6gbk
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2026-04-22に公開中

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