Literature DB >> 25981296

Role of post-translational modifications on structure, function and pharmacology of class C G protein-coupled receptors.

Lenea Nørskov-Lauritsen1, Hans Bräuner-Osborne2.   

Abstract

G protein-coupled receptors are divided into three classes (A, B and C) based on homology of their seven transmembrane domains. Class C is the smallest class with 22 human receptor subtypes including eight metabotropic glutamate (mGlu1-8) receptors, two GABAB receptors (GABAB1 and GABAB2), three taste receptors (T1R1-3), one calcium-sensing (CaS) receptor, one GPCR, class C, group 6, subtype A (GPRC6) receptor, and seven orphan receptors. G protein-coupled receptors undergo a number of post-translational modifications, which regulate their structure, function and/or pharmacology. Here, we review the existence of post-translational modifications in class C G protein-coupled receptors and their regulatory roles, with particular focus on glycosylation, phosphorylation, ubiquitination, SUMOylation, disulphide bonding and lipidation.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CaSR; GPRC6A; Glycosylation; Palmitoylation; Phosphorylation; Post-translational modifications; Ubiquitination; mGluR

Mesh:

Substances:

Year:  2015        PMID: 25981296     DOI: 10.1016/j.ejphar.2015.05.015

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


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