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Computational Identification of Novel Amino-Acid Interactions in HIV Gag via Correlated Evolution

Pairs of amino acid positions that evolve in a correlated manner are proposed to play important roles in protein structure or function. Methods to detect them might fare better with families for which sequences of thousands of closely related homologs are available than families with only a few dist...

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Detalles Bibliográficos
Autores principales: Kalinina, Olga V., Oberwinkler, Heike, Glass, Bärbel, Kräusslich, Hans-Georg, Russell, Robert B., Briggs, John A. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411748/
https://www.ncbi.nlm.nih.gov/pubmed/22879995
http://dx.doi.org/10.1371/journal.pone.0042468
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author Kalinina, Olga V.
Oberwinkler, Heike
Glass, Bärbel
Kräusslich, Hans-Georg
Russell, Robert B.
Briggs, John A. G.
author_facet Kalinina, Olga V.
Oberwinkler, Heike
Glass, Bärbel
Kräusslich, Hans-Georg
Russell, Robert B.
Briggs, John A. G.
author_sort Kalinina, Olga V.
collection PubMed
description Pairs of amino acid positions that evolve in a correlated manner are proposed to play important roles in protein structure or function. Methods to detect them might fare better with families for which sequences of thousands of closely related homologs are available than families with only a few distant relatives. We applied co-evolution analysis to thousands of sequences of HIV Gag, finding that the most significantly co-evolving positions are proximal in the quaternary structures of the viral capsid. A reduction in infectivity caused by mutating one member of a significant pair could be rescued by a compensatory mutation of the other.
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spelling pubmed-34117482012-08-09 Computational Identification of Novel Amino-Acid Interactions in HIV Gag via Correlated Evolution Kalinina, Olga V. Oberwinkler, Heike Glass, Bärbel Kräusslich, Hans-Georg Russell, Robert B. Briggs, John A. G. PLoS One Research Article Pairs of amino acid positions that evolve in a correlated manner are proposed to play important roles in protein structure or function. Methods to detect them might fare better with families for which sequences of thousands of closely related homologs are available than families with only a few distant relatives. We applied co-evolution analysis to thousands of sequences of HIV Gag, finding that the most significantly co-evolving positions are proximal in the quaternary structures of the viral capsid. A reduction in infectivity caused by mutating one member of a significant pair could be rescued by a compensatory mutation of the other. Public Library of Science 2012-08-03 /pmc/articles/PMC3411748/ /pubmed/22879995 http://dx.doi.org/10.1371/journal.pone.0042468 Text en © 2012 Kalinina et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kalinina, Olga V.
Oberwinkler, Heike
Glass, Bärbel
Kräusslich, Hans-Georg
Russell, Robert B.
Briggs, John A. G.
Computational Identification of Novel Amino-Acid Interactions in HIV Gag via Correlated Evolution
title Computational Identification of Novel Amino-Acid Interactions in HIV Gag via Correlated Evolution
title_full Computational Identification of Novel Amino-Acid Interactions in HIV Gag via Correlated Evolution
title_fullStr Computational Identification of Novel Amino-Acid Interactions in HIV Gag via Correlated Evolution
title_full_unstemmed Computational Identification of Novel Amino-Acid Interactions in HIV Gag via Correlated Evolution
title_short Computational Identification of Novel Amino-Acid Interactions in HIV Gag via Correlated Evolution
title_sort computational identification of novel amino-acid interactions in hiv gag via correlated evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411748/
https://www.ncbi.nlm.nih.gov/pubmed/22879995
http://dx.doi.org/10.1371/journal.pone.0042468
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