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  • 标题:Impact of distal mutations on the network of coupled motions correlated to hydride transfer in dihydrofolate reductase
  • 本地全文:下载
  • 作者:Kim F. Wong ; Tzvia Selzer ; Stephen J. Benkovic
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2005
  • 卷号:102
  • 期号:19
  • 页码:6807-6812
  • DOI:10.1073/pnas.0408343102
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:A comprehensive analysis of the network of coupled motions correlated to hydride transfer in dihydrofolate reductase is presented. Hybrid quantum/classical molecular dynamics simulations are combined with a rank correlation analysis method to extract thermally averaged properties that vary along the collective reaction coordinate according to a prescribed target model. Coupled motions correlated to hydride transfer are identified throughout the enzyme. Calculations for wild-type dihydrofolate reductase and a triple mutant, along with the associated single and double mutants, indicate that each enzyme system samples a unique distribution of coupled motions correlated to hydride transfer. These coupled motions provide an explanation for the experimentally measured nonadditivity effects in the hydride transfer rates for these mutants. This analysis illustrates that mutations distal to the active site can introduce nonlocal structural perturbations and significantly impact the catalytic rate by altering the conformational motions of the entire enzyme and the probability of sampling conformations conducive to the catalyzed reaction.
  • 关键词:enzyme catalysis ; molecular dynamics
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