中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Exploring the Thermodynamic Landscape, Kinetics, and Structural Evolution of a Protein Conformational Transition with a Microscopic Double-Well Model

文献类型:期刊论文

作者Lai ZZ ; Lu QA ; Wang J
刊名journal of physical chemistry b
出版日期2011
卷号115期号:14页码:4147-4159
关键词GLUTAMINE-BINDING PROTEIN ENERGY LANDSCAPE DYNAMICS MECHANISM FLUORESCENCE KINASE STATE
ISSN号1520-6106
通讯作者wang j
中文摘要functional conformational transition in the glutamine-binding protein (glnbp) is known to be the key to bind and transfer ligand glutamine. here, we developed a structure-based double-well model to investigate the thermodynamic and kinetic natures of the glnbp conformational transition. we uncovered the underlying free-energy landscape of the conformational transition with different temperatures. the analysis shows that below the melting temperature, two basins of attractions emerge, corresponding to the open state and the closed state of the protein. we explored the kinetic property of the conformational switch through the mean and distribution of the first passage time as well as the autocorrelation function. the kinetics implies the complexity and the hierarchical structure of the underlying energy landscape. we built the contact maps of the structures to probe the structural evolution of the conformational transition. finally, the phi values of the residues were calculated to identify the important residues (hot spots) of the transition state.
收录类别SCI收录期刊论文
语种英语
WOS记录号WOS:000289215600043
公开日期2012-06-11
源URL[http://ir.ciac.jl.cn/handle/322003/44706]  
专题长春应用化学研究所_长春应用化学研究所知识产出_期刊论文
推荐引用方式
GB/T 7714
Lai ZZ,Lu QA,Wang J. Exploring the Thermodynamic Landscape, Kinetics, and Structural Evolution of a Protein Conformational Transition with a Microscopic Double-Well Model[J]. journal of physical chemistry b,2011,115(14):4147-4159.
APA Lai ZZ,Lu QA,&Wang J.(2011).Exploring the Thermodynamic Landscape, Kinetics, and Structural Evolution of a Protein Conformational Transition with a Microscopic Double-Well Model.journal of physical chemistry b,115(14),4147-4159.
MLA Lai ZZ,et al."Exploring the Thermodynamic Landscape, Kinetics, and Structural Evolution of a Protein Conformational Transition with a Microscopic Double-Well Model".journal of physical chemistry b 115.14(2011):4147-4159.

入库方式: OAI收割

来源:长春应用化学研究所

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