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Residues coevolution guides the systematic identification of alternative functional conformations in proteins
Sfriso, Pedro; Duran-Frigola, Miquel; Mosca, Roberto; Emperador, Agustí; Aloy, Patrick, 1972-; Orozco López, Modesto
We present here a new approach for the systematic identification of functionally relevant conformations in proteins. Our fully automated pipeline, based on discrete molecular dynamics enriched with coevolutionary information, is able to capture alternative conformational states in 76% of the proteins studied, providing key atomic details for understanding their function and mechanism of action. We also demonstrate that, given its sampling speed, our method is well suited to explore structural transitions in a high-throughput manner, and can be used to determine functional conformational transitions at the entire proteome level.
Proteïnes
Proteòmica
Biologia molecular
Proteins
Proteomics
Molecular biology
cc-by-nc-nd (c) Elsevier B.V., 2016
info:eu-repo/semantics/embargoedAccess
http://creativecommons.org/licenses/by-nc-nd/3.0/es
Article
info:eu-repo/semantics/acceptedVersion
Elsevier B.V.
         

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