Evidence map›Paper›PMID 31615261›Full record

ArticleThe Journal of chemical physics2019

Directed kinetic transition network model.

Hongyu Zhou, Feng Wang, Doran I G Bennett, Peng Tao

Abstract read
In one paragraph

Article in The Journal of chemical physics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Analysing ill-conditioned Markov chains.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2023
    Article
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hongyu ZhouDepartment of Chemistry, Center for Scientific Computation, Center for Drug Discovery, Design, and Delivery (CD4), Southern Methodist University, Dallas, Texas 75275, USA.
Feng WangDepartment of Chemistry, Center for Scientific Computation, Center for Drug Discovery, Design, and Delivery (CD4), Southern Methodist University, Dallas, Texas 75275, USA.
Doran I G BennettDepartment of Chemistry, Center for Scientific Computation, Center for Drug Discovery, Design, and Delivery (CD4), Southern Methodist University, Dallas, Texas 75275, USA.ORCID 0000000183227371
Peng TaoDepartment of Chemistry, Center for Scientific Computation, Center for Drug Discovery, Design, and Delivery (CD4), Southern Methodist University, Dallas, Texas 75275, USA.ORCID 0000000224880239

Funding

Probing Hidden Conformational Space and Dynamical States of Circadian Clock Proteins through Rigid Residue Scan and Machine LearningR15GM122013 · NIGMS · SOUTHERN METHODIST UNIVERSITY · PI TAO, PENG · 2018 to 2023
$800k
NIGMS NIH HHS R15 GM122013
6 · The paper itself

Abstract

Molecular dynamics simulations contain detailed kinetic information related to the functional states of proteins and macromolecules, but this information is obscured by the high dimensionality of configurational space. Markov state models and transition network models are widely applied to extract kinetic descriptors from equilibrium molecular dynamics simulations. In this study, we developed the Directed Kinetic Transition Network (DKTN)-a graph representation of a master equation which is appropriate for describing nonequilibrium kinetics. DKTN models the transition rate matrix among different states under detailed balance. Adopting the mixing time from the Markov chain, we use the half mixing time as the criterion to identify critical state transition regarding the protein conformational change. The similarity between the master equation and the Kolmogorov equation suggests that the DKTN model can be reformulated into the continuous-time Markov chain model, which is a general case of the Markov chain without a specific lag time. We selected a photo-sensitive protein, vivid, as a model system to illustrate the usage of the DKTN model. Overall, the DKTN model provides a graph representation of the master equation based on chemical kinetics to model the protein conformational change without the underlying assumption of the Markovian property.

Identifiers

PMID31615261
PMCPMC6800283

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.