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QM/MM MD and Free Energy Simulation Study of Methyl Transfer Processes Catalyzed by PKMTs and PRMTs.
Chu, Yuzhuo; Guo, Hong.
Afiliação
  • Chu Y; School of Life Science and Biotechnology, Dalian University of Technology, Dalian, 116024, China. yzchu@dlut.edu.cn.
  • Guo H; Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, TN, 37996, USA.
Interdiscip Sci ; 7(3): 309-18, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26267708
Methyl transfer processes catalyzed by protein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs) control important biological events including transcriptional regulation and cell signaling. One important property of these enzymes is that different PKMTs and PRMTs catalyze the formation of different methylated product (product specificity). These different methylation states lead to different biological outcomes. Here, we review the results of quantum mechanics/molecular mechanics molecular dynamics and free energy simulations that have been performed to study the reaction mechanism of PKMTs and PRMTs and the mechanism underlying the product specificity of the methyl transfer processes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína-Arginina N-Metiltransferases / Teoria Quântica / Histona-Lisina N-Metiltransferase / Biocatálise / Simulação de Dinâmica Molecular Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína-Arginina N-Metiltransferases / Teoria Quântica / Histona-Lisina N-Metiltransferase / Biocatálise / Simulação de Dinâmica Molecular Idioma: En Ano de publicação: 2015 Tipo de documento: Article