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Evolution of Class A G-Protein-Coupled Receptors: Implications for Molecular Modeling

期刊

CURRENT MEDICINAL CHEMISTRY
卷 19, 期 8, 页码 1110-1118

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/092986712799320600

关键词

Evolution; Phylogeny; Molecular modeling; G-protein-coupled receptor; Class A GPCR; cAMP receptors; Transmembrane receptor; Protein family; Multidimensional scaling; Sequence analysis

资金

  1. CNRS
  2. INSERM
  3. University of Angers
  4. Conseil General de Maine-et-Loire
  5. INSERM - Region des Pays-de-la-Loire
  6. Association pour la Recherche sur le cancer (ARC)
  7. Centre Hospitalier Universitaire d'Angers

向作者/读者索取更多资源

Class A or rhodopsin-like G-protein-coupled receptors (GPCRs) constitute the largest transmembrane receptor family of the human genome. Because of their biological and pharmaceutical importance, the evolutionary history of these receptors has been widely studied. Most studies agree on the classification of the 700 members of this family into a dozen of sub-families. However, the relationship between these sub-families remains controversial and the molecular processes that drove the evolution and diversification of such a large family have still to be determined. We review here the evolutionary analyses carried out on class A GPCRs either by phylogenetic methods or by multidimensional scaling (MDS). We detail the key molecular events driving the evolution of this receptor family. We analyze these events in view of the recently resolved crystal structures of GPCRs and we discuss the usefulness of evolutionary information to help molecular modeling.

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