6JVU

Crystal structure of Klebsiella pneumoniae CysE in complex with L-cysteine

6JVU の概要

• エントリーDOI: 10.2210/pdb6jvu/pdb
• 分子名称: Serine acetyltransferase, 1,2-ETHANEDIOL, CYSTEINE, ... (5 entities in total)
• 機能のキーワード: serine acetyltransferase, transferase
• 由来する生物種: Klebsiella pneumoniae MGH 78578
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 182945.21

構造登録者

Verma, D.,Gupta, V. (登録日: 2019-04-17, 公開日: 2020-02-26, 最終更新日: 2023-11-22)

主引用文献

Verma, D.,Gupta, S.,Saxena, R.,Kaur, P.,R, R.,Srivastava, S.,Gupta, V.
Allosteric inhibition and kinetic characterization of Klebsiella pneumoniae CysE: An emerging drug target.
Int.J.Biol.Macromol., 151:1240-1249, 2020

PubMed Abstract: The emergence and spread of multidrug-resistant strains of Klebsiella pneumoniae is a major concern that necessitates the development of unique therapeutics. The essential requirement of serine acetyltransferase (SAT/CysE) for survival of several human pathogens makes it a very promising target for inhibitor designing and drug discovery. In this study, as an initial step to structure-based drug discovery, CysE from K. pneumonia was structurally and biochemically characterized. Subsequently, blind docking of selected natural products into the X-ray crystallography determined 3D structure of the target was carried out. Experimental validation of the inhibitory potential of the top-scorers established quercetin as an uncompetitive inhibitor of Kpn CysE. Molecular dynamics simulations carried out to elucidate the binding mode of quercetin reveal that this small molecule binds at the trimer-trimer interface of hexameric CysE, a site physically distinct from the active site of the enzyme. Detailed analysis of conformational differences incurred in Kpn CysE structure on binding to quercetin provides mechanistic understanding of allosteric modulation. Binding of quercetin to CysE leads to conformation changes in the active site loops and proximal loops that affect its internal dynamics and consequently its affinity for substrate/co-factor binding, justifying the reduced enzyme activity.

PubMed: 31751684
DOI: 10.1016/j.ijbiomac.2019.10.170

実験手法

X-RAY DIFFRACTION (2.8 Å)