Formation of Secondary and Supersecondary Structure of Proteins as a Result of Coupling Between Local and Backbone-Electrostatic Interactions: A View Through Cluster-Cumulant Scope.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2019
Historique:
entrez: 5 4 2019
pubmed: 5 4 2019
medline: 25 7 2019
Statut: ppublish

Résumé

The secondary structure of proteins results from both local and long-range interactions, the latter being primarily backbone hydrogen bonding. In this chapter, based on our recent work, we suggest that the striking regularity of secondary structure can be described, in a semi-analytical manner, in terms of Kubo cluster cumulants (corresponding to the expansion of the protein's potential of mean force) that originate from the coupling between the backbone-local and backbone-electrostatic interactions. This finding is illustrated by the analysis of the Protein Data Bank statistics. Examples demonstrating the importance of the coupling terms in coarse-grained treatment of proteins are also presented.

Identifiants

pubmed: 30945217
doi: 10.1007/978-1-4939-9161-7_7
doi:

Substances chimiques

Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Pagination

133-146

Auteurs

Adam Liwo (A)

Faculty of Chemistry, University of Gdańsk, Gdańsk, Poland. adam.liwo@ug.edu.pl.

Adam K Sieradzan (AK)

Faculty of Chemistry, University of Gdańsk, Gdańsk, Poland.

Cezary Czaplewski (C)

Faculty of Chemistry, University of Gdańsk, Gdańsk, Poland.

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Classifications MeSH