Loading
PDBj
メニューPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

4YF6

Crystal structure of oxidised Rv1284

4YF6 の概要
エントリーDOI10.2210/pdb4yf6/pdb
関連するPDBエントリー4YF4 4YF5
分子名称Beta-carbonic anhydrase 1, ZINC ION, MAGNESIUM ION, ... (5 entities in total)
機能のキーワードbeta-carbonic anhydrase, lyase
由来する生物種Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh)
タンパク質・核酸の鎖数4
化学式量合計77404.60
構造登録者
Hofmann, A. (登録日: 2015-02-25, 公開日: 2015-05-06, 最終更新日: 2024-10-30)
主引用文献Nienaber, L.,Cave-Freeman, E.,Cross, M.,Mason, L.,Bailey, U.M.,Amani, P.,A Davis, R.,Taylor, P.,Hofmann, A.
Chemical probing suggests redox-regulation of the carbonic anhydrase activity of mycobacterial Rv1284.
Febs J., 282:2708-2721, 2015
Cited by
PubMed Abstract: The mycobacterial enzyme Rv1284 is a member of the β-carbonic anhydrase family that is considered essential for survival of the pathogen. The active site cavity of this dimeric protein is characterized by an exceptionally small volume and harbours a catalytic zinc ion coordinated by two cysteine and one histidine residue side chains. Using the natural products polycarpine and emodin as chemical probes in crystallographic experiments and stopped-flow enzyme assays, we report that the catalytic activity can be reversibly inhibited by oxidation. Oxidative conditions lead to the removal of one of the active site cysteine residues from the coordination sphere of the catalytic metal ion by engagement in a disulfide bond with another cysteine residue close by. The subsequent loss of the metal ion, which is supported by crystallographic analysis, may thus render the protein catalytically inactive. The oxidative inhibition of Rv1284 can be reversed by exposing the protein to reducing conditions. Because the physical size of the chemical probes used in the present study substantially exceeds the active site volume, we hypothesized that these compounds exert their effects from a surface-bound location and identified Tyr120 as a critical residue for oxidative inactivation. These findings link conditions of oxidative stress to pH homeostasis of the pathogen. Because oxidative stress and acidification are defence mechanisms employed by the innate immune system of the host, we suggest that Rv1284 may be a component of the mycobacterial survival strategy.
PubMed: 25929542
DOI: 10.1111/febs.13313
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.002 Å)
構造検証レポート
Validation report summary of 4yf6
検証レポート(詳細版)ダウンロードをダウンロード

248942

件を2026-02-11に公開中

PDB statisticsPDBj update infoContact PDBjnumon