Role of post-translational modifications on structure, function and pharmacology of class C G protein-coupled receptors
Role of post-translational modifications on structure, function and pharmacology of class C G protein-coupled receptors
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DOI:
10.1016/j.ejphar.2015.05.015
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发表时间:
2015-09-15
影响因子:
5
通讯作者:
Brauner-Osborne, Hans
中科院分区:
文献类型:
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作者:
Norskov-Lauritsen, Lenea;Brauner-Osborne, Hans
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 (mGlu(1-8)) receptors, two GABA(B) receptors (GABA(B1) and GABA(B2)), three taste receptors (T1R1-3), one calcium-sensing (CaS) receptor, one GPCR, class C, group 6, subtype A (GPRC(6)) 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. (C) 2015 Elsevier B.V. All rights reserved.