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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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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. |
format | Online Article Text |
id | pubmed-4686048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT dassayoni diversityinproteindomainsuperfamilies AT dawsonnataliel diversityinproteindomainsuperfamilies AT orengochristinea diversityinproteindomainsuperfamilies |