4B7S

PikC D50N mutant bound to the 10-DML analog with the 3-(N,N- dimethylamino)propanoate anchoring group

4B7S の概要

• エントリーDOI: 10.2210/pdb4b7s/pdb
• 関連するPDBエントリー: 2BVJ 2C6H 2C7X 2CA0 2CD8 2VZ7 2VZM 2WHW 2WI9 3ZK5 4B7D
• 分子名称: CYTOCHROME P450 HYDROXYLASE PIKC, PROTOPORPHYRIN IX CONTAINING FE, SULFATE ION, ... (6 entities in total)
• 機能のキーワード: oxidoreductase, monooxygenase, pikromycin biosynthesis, inhibitor
• 由来する生物種: STREPTOMYCES VENEZUELAE
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 99972.72

構造登録者

Podust, L.M. (登録日: 2012-08-21, 公開日: 2013-08-28, 最終更新日: 2023-12-20)

主引用文献

Negretti, S.,Narayan, A.R.H.,Chiou, K.C.,Kells, P.M.,Stachowski, J.L.,Hansen, D.A.,Podust, L.M.,Montgomery, J.,Sherman, D.H.
Directing Group-Controlled Regioselectivity in an Enzymatic C-H Bond Oxygenation.
J.Am.Chem.Soc., 136:4901-, 2014

PubMed Abstract: Highly regioselective remote hydroxylation of a natural product scaffold is demonstrated by exploiting the anchoring mechanism of the biosynthetic P450 monooxygenase PikCD50N-RhFRED. Previous studies have revealed structural and biochemical evidence for the role of a salt bridge between the desosamine N,N-dimethylamino functionality of the natural substrate YC-17 and carboxylate residues within the active site of the enzyme, and selectivity in subsequent C-H bond functionalization. In the present study, a substrate-engineering approach was conducted that involves replacing desosamine with varied synthetic N,N-dimethylamino anchoring groups. We then determined their ability to mediate enzymatic total turnover numbers approaching or exceeding that of the natural sugar, while enabling ready introduction and removal of these amino anchoring groups from the substrate. The data establish that the size, stereochemistry, and rigidity of the anchoring group influence the regioselectivity of enzymatic hydroxylation. The natural anchoring group desosamine affords a 1:1 mixture of regioisomers, while synthetic anchors shift YC-17 analogue C-10/C-12 hydroxylation from 20:1 to 1:4. The work demonstrates the utility of substrate engineering as an orthogonal approach to protein engineering for modulation of regioselective C-H functionalization in biocatalysis.

PubMed: 24627965
DOI: 10.1021/JA5016052

実験手法

X-RAY DIFFRACTION (1.84 Å)