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Protein sectors: statistical coupling analysis versus conservation.
Tesileanu, Tiberiu; Colwell, Lucy J; Leibler, Stanislas.
Afiliación
  • Tesileanu T; The Simons Center for Systems Biology and The School of Natural Sciences, Institute for Advanced Study, Einstein Drive, Princeton, New Jersey, United States of America; Initiative for the Theoretical Sciences, CUNY Graduate Center, 365 Fifth Avenue, New York, New York, United States of America.
  • Colwell LJ; The Simons Center for Systems Biology and The School of Natural Sciences, Institute for Advanced Study, Einstein Drive, Princeton, New Jersey, United States of America; Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, United Kingdom.
  • Leibler S; The Simons Center for Systems Biology and The School of Natural Sciences, Institute for Advanced Study, Einstein Drive, Princeton, New Jersey, United States of America; Center for Studies in Physics and Biology and Laboratory of Living Matter, The Rockefeller University, 1230 York Avenue, New York, New York, United States of America.
PLoS Comput Biol ; 11(2): e1004091, 2015 Feb.
Article en En | MEDLINE | ID: mdl-25723535
ABSTRACT
Statistical coupling analysis (SCA) is a method for analyzing multiple sequence alignments that was used to identify groups of coevolving residues termed "sectors". The method applies spectral analysis to a matrix obtained by combining correlation information with sequence conservation. It has been asserted that the protein sectors identified by SCA are functionally significant, with different sectors controlling different biochemical properties of the protein. Here we reconsider the available experimental data and note that it involves almost exclusively proteins with a single sector. We show that in this case sequence conservation is the dominating factor in SCA, and can alone be used to make statistically equivalent functional predictions. Therefore, we suggest shifting the experimental focus to proteins for which SCA identifies several sectors. Correlations in protein alignments, which have been shown to be informative in a number of independent studies, would then be less dominated by sequence conservation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas / Alineación de Secuencia / Biología Computacional / Análisis de Secuencia de Proteína / Dominios y Motivos de Interacción de Proteínas Tipo de estudio: Prognostic_studies Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas / Alineación de Secuencia / Biología Computacional / Análisis de Secuencia de Proteína / Dominios y Motivos de Interacción de Proteínas Tipo de estudio: Prognostic_studies Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos