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Adhesion G Protein-coupled Receptors

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Cover of 'Adhesion G Protein-coupled Receptors'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction: History of the Adhesion GPCR Field.
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    Chapter 2 Classification, Nomenclature, and Structural Aspects of Adhesion GPCRs.
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    Chapter 3 7TM Domain Structure of Adhesion GPCRs.
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    Chapter 4 Understanding the Structural Basis of Adhesion GPCR Functions.
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    Chapter 5 Control of Adhesion GPCR Function Through Proteolytic Processing.
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    Chapter 6 Tethered Agonism: A Common Activation Mechanism of Adhesion GPCRs.
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    Chapter 7 Versatile Signaling Activity of Adhesion GPCRs.
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    Chapter 8 Adhesion G Protein-coupled Receptors
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    Chapter 9 The Relevance of Genomic Signatures at Adhesion GPCR Loci in Humans.
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    Chapter 10 Adhesion GPCRs as a Putative Class of Metabotropic Mechanosensors.
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    Chapter 11 Adhesion GPCRs Govern Polarity of Epithelia and Cell Migration.
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    Chapter 12 Adhesion GPCRs as Novel Actors in Neural and Glial Cell Functions: From Synaptogenesis to Myelination.
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    Chapter 13 Control of Skeletal Muscle Cell Growth and Size Through Adhesion GPCRs.
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    Chapter 14 Adhesion GPCR Function in Pulmonary Development and Disease.
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    Chapter 15 Adhesion GPCRs as Modulators of Immune Cell Function.
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    Chapter 16 Heart Development, Angiogenesis, and Blood-Brain Barrier Function Is Modulated by Adhesion GPCRs.
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    Chapter 17 Adhesion GPCRs in Tumorigenesis.
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    Chapter 18 Erratum to: 7TM Domain Structure of Adhesion GPCRs
Attention for Chapter 7: Versatile Signaling Activity of Adhesion GPCRs.
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Chapter title
Versatile Signaling Activity of Adhesion GPCRs.
Chapter number 7
Book title
Adhesion G Protein-coupled Receptors
Published in
Handbook of experimental pharmacology, November 2016
DOI 10.1007/978-3-319-41523-9_7
Pubmed ID
Book ISBNs
978-3-31-941521-5, 978-3-31-941523-9
Authors

Ayush Kishore, Randy A. Hall

Editors

Tobias Langenhan, Torsten Schöneberg

Abstract

The adhesion G protein-coupled receptors (aGPCRs) are a family of 33 receptors in humans that are widely expressed in various tissues and involved in many diverse biological processes. These receptors possess extremely large N-termini (NT) containing a variety of adhesion domains. A distinguishing feature of these receptors is the presence within the NT of a highly conserved GPCR autoproteolysis-inducing (GAIN) domain, which mediates autoproteolysis of the receptors into N-terminal and C-terminal fragments that stay non-covalently associated. The downstream signaling pathways and G protein-coupling preferences of many aGPCRs have recently been elucidated, and putative endogenous ligands for some aGPCRs have also been discovered and characterized in recent years. A pivotal observation for aGPCRs has been that deletion or removal of the NT up the point of GAIN cleavage results in constitutive receptor activation. For at least some aGPCRs, this activation is dependent on the unmasking of specific agonistic peptide sequences within the N-terminal stalk region (i.e., the region between the site of GAIN domain cleavage and the first transmembrane domain). However, the specific peptide sequences involved and the overall importance of the stalk region for activation can vary greatly from receptor to receptor. An emerging theme of work in this area is that aGPCRs are capable of versatile signaling activity that may be fine-tuned to suit the specific physiological roles played by the various members of this family.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 14 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 21%
Student > Master 2 14%
Student > Bachelor 2 14%
Other 1 7%
Lecturer > Senior Lecturer 1 7%
Other 0 0%
Unknown 5 36%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 29%
Pharmacology, Toxicology and Pharmaceutical Science 1 7%
Agricultural and Biological Sciences 1 7%
Immunology and Microbiology 1 7%
Psychology 1 7%
Other 1 7%
Unknown 5 36%