Multiscale Computational Study of the Conformation of the Full-Length Intrinsically Disordered Protein MeCP2-Reference-Cited by-同舟云学术

Multiscale Computational Study of the Conformation of the Full-Length Intrinsically Disordered Protein MeCP2

Published:2022-02-07 Issue:4 Volume:62 Page:958-970
ISSN:1549-9596
Container-title:Journal of Chemical Information and Modeling
language:en
Short-container-title:J. Chem. Inf. Model.

Author:

Chávez-García Cecilia¹²,Hénin Jérôme³,Karttunen Mikko¹²⁴^ORCID

Affiliation:

1. Department of Chemistry, the University of Western Ontario, 1151 Richmond Street, London, Ontario N6A 5B7, Canada

2. The Centre of Advanced Materials and Biomaterials Research, the University of Western Ontario, 1151 Richmond Street, London, Ontario N6A 5B7, Canada

3. Laboratoire de Biochimie Théorique UPR 9080, CNRS and Université de Paris, Paris 75005, France

4. Department of Physics and Astronomy, the University of Western Ontario, 1151 Richmond Street, London, Ontario N6A 3K7, Canada

Funder

Agence Nationale de la Recherche

Canada Research Chairs

Natural Sciences and Engineering Research Council of Canada

Ontario Trillium Foundation

Laboratoire International Associ? CNRS/UIUC

Publisher

American Chemical Society (ACS)

Subject

Library and Information Sciences,Computer Science Applications,General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jcim.1c01354

Reference58 articles.

1. Intrinsic Disorder and Autonomous Domain Function in the Multifunctional Nuclear Protein, MeCP2

2. The solution structure of the domain from MeCP2 that binds to methylated DNA

3. Recent advances in MeCP2 structure and functionThis paper is one of a selection of papers published in this Special Issue, entitled 29th Annual International Asilomar Chromatin and Chromosomes Conference, and has undergone the Journal’s usual peer review process.

4. DNA Binding Restricts the Intrinsic Conformational Flexibility of Methyl CpG Binding Protein 2 (MeCP2)

5. Coil-to-helix transitions in intrinsically disordered methyl CpG binding protein 2 and its isolated domains

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