Results 11 to 20 of about 584,709 (292)

Targeting G protein–coupled receptor kinases to G protein–coupled receptors

open access: yesCurrent Opinion in Endocrine and Metabolic Research, 2021
G protein-coupled receptors (GPCRs) interact with three protein families following agonist binding: heterotrimeric G proteins, G protein-coupled receptor kinases (GRKs) and arrestins. GRK-mediated phosphorylation of GPCRs promotes arrestin binding to uncouple the receptor from G protein, a process called desensitization, and for many GPCRs, arrestin ...
Jeffrey L. Benovic, Sarah M. Sulon
openaire   +4 more sources

G-Protein-Coupled Receptors

open access: yesBritish Journal of Pharmacology, 2011
Receptors coupled to heterotrimeric guanine nucleotide-binding proteins, the socalled G-protein-coupled receptors (GPCR), represent the largest set of plasmalemmal ...
S P H Alexander   +2 more
openaire   +5 more sources

G-protein-coupled receptors at a glance [PDF]

open access: yesJournal of Cell Science, 2003
[No abstract available]
Douglas J. Sheffler   +2 more
openaire   +3 more sources

G Protein–Coupled Receptor Heteromers [PDF]

open access: yesAnnual Review of Pharmacology and Toxicology, 2016
G protein–coupled receptors (GPCRs) compose one of the largest families of membrane proteins involved in intracellular signaling. They are involved in numerous physiological and pathological processes and are prime candidates for drug development. Over the past decade, an increasing number of studies have reported heteromerization between GPCRs.
Wakako Fujita   +6 more
openaire   +4 more sources

G Protein-Coupled Receptors in Cancer [PDF]

open access: yesInternational Journal of Molecular Sciences, 2016
Despite the fact that G protein-coupled receptors (GPCRs) are the largest signal-conveying receptor family and mediate many physiological processes, their role in tumor biology is underappreciated. Numerous lines of evidence now associate GPCRs and their downstream signaling targets in cancer growth and development.
Beatrice Uziely   +6 more
openaire   +3 more sources

Evolution of vertebrate GnRH receptors from the perspective of a basal vertebrate

open access: yesFrontiers in Endocrinology, 2012
This minireview provides the current status on gonadotropin-releasing hormone receptors (GnRH-R) in vertebrates, from the perspective of a basal vertebrate, the sea lamprey, and provides an evolutionary scheme based on the recent advance of whole genome ...
Stacia A Sower   +3 more
doaj   +1 more source

G Protein-Coupled Receptors: Undervalued Targets for Cancer Therapy

open access: yesIraqi Journal of Pharmaceutical Sciences, 2022
Despite the G protein-coupled receptors (GPCRs) being the largest family of signalling proteins at the surface of cells, their potential to be targeted in cancer therapy is still under-utilised.
Ismail Ibrahim Al-Janabi
doaj   +1 more source

Interaction of the Xanthine Nucleotide Binding Goα Mutant with G Protein-coupled Receptors [PDF]

open access: yes, 1998
We constructed a double mutant version of the α subunit of Go that was regulated by xanthine nucleotides instead of guanine nucleotides (GoαX). We investigated the interaction between GoαX and G protein-coupled receptors in vitro.
Simon, Melvin I., Yu, Bo
core   +1 more source

Current applications of mini G proteins to study the structure and function of G protein-coupled receptors [PDF]

open access: yes, 2018
G protein-coupled receptors (GPCRs) regulate intracellular signalling pathways that contribute to virtually all aspects of cell function. Characterising GPCRs in each of their conformational states is key to understanding their mechanism of action, but ...
Carpenter, Byron
core   +1 more source

Neuropeptide G Protein-Coupled Receptors as Oncotargets

open access: yesFrontiers in Endocrinology, 2018
Neuropeptide G protein-coupled receptors (GPCRs) are overexpressed on numerous cancer cells. In a number of tumors, such as small cell lung cancer (SCLC), bombesin (BB) like peptides and neurotensin (NTS) function as autocrine growth factors whereby they
Terry W. Moody   +2 more
doaj   +1 more source

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