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构建图表以描述d-丙氨酸:d-乳酸连接酶VanA中的动力学、动力学和能量学。

Building Graphs To Describe Dynamics, Kinetics, and Energetics in the d-ALa:d-Lac Ligase VanA.

作者信息

Duclert-Savatier Nathalie, Bouvier Guillaume, Nilges Michael, Malliavin Thérèse E

机构信息

Département de Biologie Structurale et Chimie, Institut Pasteur, Unité de Bioinformatique Structurale, CNRS UMR 3528 , 25, rue du Dr Roux, 75015 Paris, France.

出版信息

J Chem Inf Model. 2016 Sep 26;56(9):1762-75. doi: 10.1021/acs.jcim.6b00211. Epub 2016 Sep 12.

Abstract

The d-Ala:d-Lac ligase, VanA, plays a critical role in the resistance of vancomycin. Indeed, it is involved in the synthesis of a peptidoglycan precursor, to which vancomycin cannot bind. The reaction catalyzed by VanA requires the opening of the so-called "ω-loop", so that the substrates can enter the active site. Here, the conformational landscape of VanA is explored by an enhanced sampling approach: the temperature-accelerated molecular dynamics (TAMD). Analysis of the molecular dynamics (MD) and TAMD trajectories recorded on VanA permits a graphical description of the structural and kinetics aspects of the conformational space of VanA, where the internal mobility and various opening modes of the ω-loop play a major role. The other important feature is the correlation of the ω-loop motion with the movements of the opposite domain, defined as containing the residues A149-Q208. Conformational and kinetic clusters have been determined and a path describing the ω-loop opening was extracted from these clusters. The determination of this opening path, as well as the relative importance of hydrogen bonds along the path, permit one to propose some key residue interactions for the kinetics of the ω-loop opening.

摘要

D-丙氨酸:D-乳酸连接酶VanA在万古霉素耐药性中起着关键作用。实际上,它参与了一种肽聚糖前体的合成,而万古霉素无法与该前体结合。VanA催化的反应需要所谓的“ω-环”打开,以便底物能够进入活性位点。在此,通过一种增强采样方法——温度加速分子动力学(TAMD)来探索VanA的构象景观。对VanA记录的分子动力学(MD)和TAMD轨迹进行分析,可以对VanA构象空间的结构和动力学方面进行图形化描述,其中ω-环的内部流动性和各种打开模式起着主要作用。另一个重要特征是ω-环运动与相对结构域(定义为包含残基A149-Q208)运动的相关性。已经确定了构象和动力学簇,并从这些簇中提取了一条描述ω-环打开的路径。这条打开路径的确定以及沿路径氢键的相对重要性,使人们能够提出一些关于ω-环打开动力学的关键残基相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d40/5039762/3f12a0ed32d7/ci-2016-00211r_0001.jpg

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