7WYG
Crystal structure of P450BSbeta-L78I/Q85H/G290I variant in complex with palmitic acid.
7WYG の概要
| エントリーDOI | 10.2210/pdb7wyg/pdb |
| 分子名称 | Cytochrome P450 152A1, PROTOPORPHYRIN IX CONTAINING FE, PALMITOLEIC ACID, ... (6 entities in total) |
| 機能のキーワード | cytochrome p450, oxidoreductase |
| 由来する生物種 | Bacillus subtilis |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 99624.24 |
| 構造登録者 | |
| 主引用文献 | Zhang, K.,Yu, A.,Chu, X.,Li, F.,Liu, J.,Liu, L.,Bai, W.J.,He, C.,Wang, X. Biocatalytic Enantioselective beta-Hydroxylation of Unactivated C-H Bonds in Aliphatic Carboxylic Acids. Angew.Chem.Int.Ed.Engl., 61:e202204290-e202204290, 2022 Cited by PubMed Abstract: Catalytic selective hydroxylation of unactivated aliphatic (sp ) C-H bonds without a directing group represents a formidable task for synthetic chemists. Through directed evolution of P450 hydroxylase, we realize oxyfunctionalization of unactivated C-H bonds in a broad spectrum of aliphatic carboxylic acids with varied chain lengths, functional groups and (hetero-)aromatic moieties in a highly chemo-, regio- and enantioselective fashion (>30 examples, Cβ/Cα>20 : 1, >99 % ee). The X-ray structure of the evolved variant, P450 -L78I/Q85H/G290I, in complex with palmitic acid well rationalizes the experimentally observed regio- and enantioselectivity, and also reveals a reduced catalytic pocket volume that accounts for the increased reactivity with smaller substrates. This work showcases the potential of employing a biocatalyst to enable a chemical transformation that is particularly challenging by chemical methods. PubMed: 35536725DOI: 10.1002/anie.202204290 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2 Å) |
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