2X23

crystal structure of M. tuberculosis InhA inhibited by PT70

2X23 の概要

• エントリーDOI: 10.2210/pdb2x23/pdb
• 関連するPDBエントリー: 1BVR 1ENY 1ENZ 1P44 1P45 1ZID 2AQI 2AQK 2B35 2B36 2B37 2H7I 2H7M 2H7P 2NV6 2X22
• 分子名称: ENOYL-[ACYL-CARRIER-PROTEIN] REDUCTASE [NADH], NICOTINAMIDE-ADENINE-DINUCLEOTIDE, 5-HEXYL-2-(2-METHYLPHENOXY)PHENOL, ... (5 entities in total)
• 機能のキーワード: fatty acid biosynthesis, oxidoreductase, lipid synthesis, antibiotic resistance
• 由来する生物種: MYCOBACTERIUM TUBERCULOSIS
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 118088.53

構造登録者

Luckner, S.R.,Liu, N.,am Ende, C.W.,Tonge, P.J.,Kisker, C. (登録日: 2010-01-10, 公開日: 2010-03-02, 最終更新日: 2024-05-08)

主引用文献

Luckner, S.R.,Liu, N.,Am Ende, C.W.,Tonge, P.J.,Kisker, C.
A Slow, Tight Binding Inhibitor of Inha, the Enoyl-Acyl Carrier Protein Reductase from Mycobacterium Tuberculosis.
J.Biol.Chem., 285:14330-, 2010

PubMed Abstract: InhA, the enoyl-ACP reductase in Mycobacterium tuberculosis is an attractive target for the development of novel drugs against tuberculosis, a disease that kills more than two million people each year. InhA is the target of the current first line drug isoniazid for the treatment of tuberculosis infections. Compounds that directly target InhA and do not require activation by the mycobacterial catalase-peroxidase KatG are promising candidates for treating infections caused by isoniazid-resistant strains. Previously we reported the synthesis of several diphenyl ethers with nanomolar affinity for InhA. However, these compounds are rapid reversible inhibitors of the enzyme, and based on the knowledge that long drug target residence times are an important factor for in vivo drug activity, we set out to generate a slow onset inhibitor of InhA using structure-based drug design. 2-(o-Tolyloxy)-5-hexylphenol (PT70) is a slow, tight binding inhibitor of InhA with a K(1) value of 22 pm. PT70 binds preferentially to the InhA x NAD(+) complex and has a residence time of 24 min on the target, which is 14,000 times longer than that of the rapid reversible inhibitor from which it is derived. The 1.8 A crystal structure of the ternary complex between InhA, NAD(+), and PT70 reveals the molecular details of enzyme-inhibitor recognition and supports the hypothesis that slow onset inhibition is coupled to ordering of an active site loop, which leads to the closure of the substrate-binding pocket.

PubMed: 20200152
DOI: 10.1074/JBC.M109.090373

実験手法

X-RAY DIFFRACTION (1.807 Å)