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Diversity in protein domain superfamilies

Whilst ∼93% of domain superfamilies appear to be relatively structurally and functionally conserved based on the available data from the CATH-Gene3D domain classification resource, the remainder are much more diverse. In this review, we consider how domains in some of the most ubiquitous and promisc...

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Autores principales: Das, Sayoni, Dawson, Natalie L, Orengo, Christine A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686048/
https://www.ncbi.nlm.nih.gov/pubmed/26451979
http://dx.doi.org/10.1016/j.gde.2015.09.005
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author Das, Sayoni
Dawson, Natalie L
Orengo, Christine A
author_facet Das, Sayoni
Dawson, Natalie L
Orengo, Christine A
author_sort Das, Sayoni
collection PubMed
description Whilst ∼93% of domain superfamilies appear to be relatively structurally and functionally conserved based on the available data from the CATH-Gene3D domain classification resource, the remainder are much more diverse. In this review, we consider how domains in some of the most ubiquitous and promiscuous superfamilies have evolved, in particular the plasticity in their functional sites and surfaces which expands the repertoire of molecules they interact with and actions performed on them. To what extent can we identify a core function for these superfamilies which would allow us to develop a ‘domain grammar of function’ whereby a protein's biological role can be proposed from its constituent domains? Clearly the first step is to understand the extent to which these components vary and how changes in their molecular make-up modifies function.
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spelling pubmed-46860482016-01-15 Diversity in protein domain superfamilies Das, Sayoni Dawson, Natalie L Orengo, Christine A Curr Opin Genet Dev Article Whilst ∼93% of domain superfamilies appear to be relatively structurally and functionally conserved based on the available data from the CATH-Gene3D domain classification resource, the remainder are much more diverse. In this review, we consider how domains in some of the most ubiquitous and promiscuous superfamilies have evolved, in particular the plasticity in their functional sites and surfaces which expands the repertoire of molecules they interact with and actions performed on them. To what extent can we identify a core function for these superfamilies which would allow us to develop a ‘domain grammar of function’ whereby a protein's biological role can be proposed from its constituent domains? Clearly the first step is to understand the extent to which these components vary and how changes in their molecular make-up modifies function. Elsevier 2015-12 /pmc/articles/PMC4686048/ /pubmed/26451979 http://dx.doi.org/10.1016/j.gde.2015.09.005 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Das, Sayoni
Dawson, Natalie L
Orengo, Christine A
Diversity in protein domain superfamilies
title Diversity in protein domain superfamilies
title_full Diversity in protein domain superfamilies
title_fullStr Diversity in protein domain superfamilies
title_full_unstemmed Diversity in protein domain superfamilies
title_short Diversity in protein domain superfamilies
title_sort diversity in protein domain superfamilies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686048/
https://www.ncbi.nlm.nih.gov/pubmed/26451979
http://dx.doi.org/10.1016/j.gde.2015.09.005
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