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Adhesion Class GPCRs (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database

Authors :
Torsten Schöneberg
Diana Le Duc
Breanne L. Harty
Christiane Kirchhoff
Simone Prömel
Heike Cappallo-Obermann
Demet Arac-Ozkan
Xianhua Piao
Gabriela Aust
Lei Xu
Helgi B. Schiöth
Hsi-Hsien Lin
Kathleen Singer
Barbara Knapp
Uwe Wolfrum
Jörg Hamann
Arunkumar Krishnan
Martin Stacey
Henrike O. Heyne
Tobias Langenhan
David C. Martinelli
Caroline J. Formstone
Yuri A. Ushkaryov
Tom I. Bonner
Kelly Monk
Source :
IUPHAR/BPS Guide to Pharmacology CITE. 2019
Publication Year :
2019
Publisher :
Edinburgh University Library, 2019.

Abstract

Adhesion GPCRs are structurally identified on the basis of a large extracellular region, similar to the Class B GPCR, but which is linked to the 7TM region by a GPCR autoproteolysis-inducing (GAIN) domain [8] containing a GPCR proteolytic site. The N-terminus often shares structural homology with adhesive domains (e.g. cadherins, immunolobulin, lectins) facilitating inter- and matricellular interactions and leading to the term adhesion GPCR [82, 332]. Several receptors have been suggested to function as mechanosensors [254, 234, 315, 32]. The nomenclature of these receptors was revised in 2015 as recommended by NC-IUPHAR and the Adhesion GPCR Consortium [100].

Details

ISSN :
26331020
Volume :
2019
Database :
OpenAIRE
Journal :
IUPHAR/BPS Guide to Pharmacology CITE
Accession number :
edsair.doi...........2c6c2fe20a12572da6bb8aa516cf7e48