Multimodal Structural Distribution of the p53 C-Terminal Domain upon Binding to S100B via a Generalized Ensemble Method: From Disorder to Extradisorder-Reference-Cited by-同舟云学术

Multimodal Structural Distribution of the p53 C-Terminal Domain upon Binding to S100B via a Generalized Ensemble Method: From Disorder to Extradisorder

Published:2019-03-11 Issue:4 Volume:15 Page:2597-2607
ISSN:1549-9618
Container-title:Journal of Chemical Theory and Computation
language:en
Short-container-title:J. Chem. Theory Comput.

Author:

Iida Shinji¹,Kawabata Takeshi¹,Kasahara Kota²^ORCID,Nakamura Haruki¹,Higo Junichi³^ORCID

Affiliation:

1. Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka 565-0871, Japan

2. College of Life Sciences, Ritsumeikan University, Noji-higashi 1-1-1, Kusatsu, Shiga 525-8577, Japan

3. Graduate School of Simulation Studies, University of Hyogo, 7-1-28 Minatojima-Minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan

Funder

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

Institute for Protein Research, Osaka University

High-Performance Computing Infrastructure

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry,Computer Science Applications

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jctc.8b01042

Reference73 articles.

1. Hub Promiscuity in Protein-Protein Interaction Networks

2. Intrinsic Disorder Is a Common Feature of Hub Proteins from Four Eukaryotic Interactomes

3. Classification of Intrinsically Disordered Regions and Proteins

4. Mechanism of coupled folding and binding of an intrinsically disordered protein

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