QM-MM investigation on chorismate synthase enzyme role

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...

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主要作者: Lawan,N.
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出版: Chiang Mai University 2015
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spelling th-cmuir.6653943832-387532015-06-16T07:54:08Z QM-MM investigation on chorismate synthase enzyme role Lawan,N. Physics and Astronomy (all) Chemistry (all) Materials Science (all) Mathematics (all) Biochemistry, Genetics and Molecular Biology (all) 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. 2015-06-16T07:54:08Z 2015-06-16T07:54:08Z 2014-01-01 Article 01252526 2-s2.0-84905722622 http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84905722622&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38753 Chiang Mai University
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Physics and Astronomy (all)
Chemistry (all)
Materials Science (all)
Mathematics (all)
Biochemistry, Genetics and Molecular Biology (all)
spellingShingle Physics and Astronomy (all)
Chemistry (all)
Materials Science (all)
Mathematics (all)
Biochemistry, Genetics and Molecular Biology (all)
Lawan,N.
QM-MM investigation on chorismate synthase enzyme role
description 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.
format Article
author Lawan,N.
author_facet Lawan,N.
author_sort Lawan,N.
title QM-MM investigation on chorismate synthase enzyme role
title_short QM-MM investigation on chorismate synthase enzyme role
title_full QM-MM investigation on chorismate synthase enzyme role
title_fullStr QM-MM investigation on chorismate synthase enzyme role
title_full_unstemmed QM-MM investigation on chorismate synthase enzyme role
title_sort qm-mm investigation on chorismate synthase enzyme role
publisher Chiang Mai University
publishDate 2015
url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84905722622&origin=inward
http://cmuir.cmu.ac.th/handle/6653943832/38753
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