QM-MM Investigation on Chorismate Synthase Enzyme Role

被引:0
|
作者
Lawan, Narin [1 ]
机构
[1] Chiang Mai Univ, Fac Sci, Dept Chem, CSML, Chiang Mai 50200, Thailand
来源
CHIANG MAI JOURNAL OF SCIENCE | 2014年 / 41卷 / 03期
关键词
chorismate synthase; enzyme role; QM-MM method; transition state and product stabilization; TRANSITION-STATE STABILIZATION; MYCOBACTERIUM-TUBERCULOSIS; ACTIVE-SITE; SUBSTRATE; MUTASE; CATALYSIS; PROTEINS; RESIDUES; DYNAMICS; MODEL;
D O I
暂无
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chorismate is a key intermediate in the biosynthesis of many aromatic compounds, including the aromatic amino acids. Chorismate synthase (CS) is an enzyme responsible for the biosynthesis of chorismate. Although several proposals have been made, the role of this enzyme is still unclear. In this work, therefore, the QM-MM adiabatic mapping calculations at the AM1-CHARMM27 level were performed. The comparisons between potential energy surface (PES) of reaction in enzyme (QM-MM energy) and the PES of reaction without enzyme (QM energy) were made. The results showed that the first step of the reaction mechanism is proton transfer rather than phosphate elimination. Several mechanisms have been proposed that the CS enzyme stabilized transition state to catalyze the reaction. This work, however, observed that not only was transition state stabilized but also intermediate and product. In addition, the enzyme holds substrate and cofactor together in the appropriate orientation making the reaction easier to proceed.
引用
收藏
页码:618 / 626
页数:9
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