4MQP

Mycobaterium tuberculosis transaminase BioA complexed with 2-hydrazinylbenzo[d]thiazole

4MQP の概要

• エントリーDOI: 10.2210/pdb4mqp/pdb
• 関連するPDBエントリー: 4MQN 4MQO 4MQQ 4MQR
• 分子名称: Adenosylmethionine-8-amino-7-oxononanoate aminotransferase, (4-{[(E)-1,3-benzothiazol-2-yldiazenyl]methyl}-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate, 1,2-ETHANEDIOL, ... (5 entities in total)
• 機能のキーワード: plp, transaminase, transferase
• 由来する生物種: Mycobacterium tuberculosis
• 細胞内の位置: Cytoplasm (By similarity): P0A4X6
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 98154.05

構造登録者

Finzel, B.C.,Dai, R. (登録日: 2013-09-16, 公開日: 2014-03-05, 最終更新日: 2023-09-20)

主引用文献

Dai, R.,Wilson, D.J.,Geders, T.W.,Aldrich, C.C.,Finzel, B.C.
Inhibition of Mycobacterium tuberculosis Transaminase BioA by Aryl Hydrazines and Hydrazides.
Chembiochem, 15:575-586, 2014

PubMed Abstract: 7,8-Diaminopelargonic acid synthase (BioA) of Mycobacterium tuberculosis is a recently validated target for therapeutic intervention in the treatment of tuberculosis (TB). Using biophysical fragment screening and structural characterization of compounds, we have identified a potent aryl hydrazine inhibitor of BioA that reversibly modifies the pyridoxal-5'-phosphate (PLP) cofactor, forming a stable quinonoid. Analogous hydrazides also form covalent adducts that can be observed crystallographically but are incapable of inactivating the enzyme. In the X-ray crystal structures, small molecules induce unexpected conformational remodeling in the substrate binding site. We compared these conformational changes to those induced upon binding of the substrate (7-keto-8-aminopelargonic acid), and characterized the inhibition kinetics and the X-ray crystal structures of BioA with the hydrazine compound and analogues to unveil the mechanism of this reversible covalent modification.

PubMed: 24482078
DOI: 10.1002/cbic.201300748

実験手法

X-RAY DIFFRACTION (1.83 Å)