4YPO

Crystal structure of Mycobacterium tuberculosis ketol-acid reductoisomerase in complex with Mg2+

4YPO の概要

• エントリーDOI: 10.2210/pdb4ypo/pdb
• 分子名称: Ketol-acid reductoisomerase, MAGNESIUM ION, CHLORIDE ION, ... (5 entities in total)
• 機能のキーワード: ilvc, branch chain amino acids, knotted protein, rossmann fold, oxidoreductase
• 由来する生物種: Mycobacterium tuberculosis
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 72677.91

構造登録者

Lv, Y.,Guddat, L.W. (登録日: 2015-03-13, 公開日: 2016-02-17, 最終更新日: 2024-02-28)

主引用文献

Lv, Y.,Kandale, A.,Wun, S.J.,McGeary, R.P.,Williams, S.J.,Kobe, B.,Sieber, V.,Schembri, M.A.,Schenk, G.,Guddat, L.W.
Crystal structure of Mycobacterium tuberculosis ketol-acid reductoisomerase at 1.0 angstrom resolution - a potential target for anti-tuberculosis drug discovery.
Febs J., 283:1184-1196, 2016

PubMed Abstract: The biosynthetic pathway for the branched-chain amino acids is present in plants, fungi and bacteria, but not in animals, making it an attractive target for herbicidal and antimicrobial drug discovery. Ketol-acid reductoisomerase (KARI; EC 1.1.1.86) is the second enzyme in this pathway, converting in a Mg(2+) - and NADPH-dependent reaction either 2-acetolactate or 2-aceto-2-hydroxybutyrate to their corresponding 2,3-dihydroxy-3-alkylbutyrate products. Here, we have determined the crystal structure of Mycobacterium tuberculosis (Mt) KARI, a class I KARI, with two magnesium ions bound in the active site. X-ray data were obtained to 1.0 Å resolution and the final model has an Rfree of 0.163. The structure shows that the active site is solvent-accessible with the two metal ions separated by 4.7 Å. A comparison of this structure with that of Mg(2+) -free Pseudomonas aeruginosa KARI suggests that upon magnesium binding no movement of the N domain relative to the C domain occurs. However, upon formation of the Michaelis complex, as illustrated in the structure of Slackia exigua KARI in complex with NADH.Mg(2+) . N-hydroxy-N-isopropyloxamate (IpOHA, a transition state analog), domain movements and reduction of the metal-metal distance to 3.5 Å are observed. This inherent flexibility therefore appears to be critical for initiation of the KARI-catalyzed reaction. This study provides new insights into the complex structural rearrangements required for activity of KARIs, particularly those belonging to class I, and provides the framework for the rational design of Mt KARI inhibitors that can be tested as novel antituberculosis agents.

PubMed: 26876563
DOI: 10.1111/febs.13672

実験手法

X-RAY DIFFRACTION (1.001 Å)