Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1991 Dec 15;88(24):11067-70.
doi: 10.1073/pnas.88.24.11067.

Isolation of Drosophila genes encoding G protein-coupled receptor kinases

Affiliations
Comparative Study

Isolation of Drosophila genes encoding G protein-coupled receptor kinases

J A Cassill et al. Proc Natl Acad Sci U S A. .

Abstract

G protein-coupled receptors are regulated via phosphorylation by a variety of protein kinases. Recently, termination of the active state of two such receptors, the beta-adrenergic receptor and rhodopsin, has been shown to be mediated by agonist- or light-dependent phosphorylation of the receptor by members of a family of protein-serine/threonine kinases (here referred to as G protein-coupled receptor kinases). We now report the isolation of a family of genes encoding a set of Drosophila protein kinases that appear to code for G protein-coupled receptor kinases. These proteins share a high degree of sequence homology with the bovine beta-adrenergic receptor kinase. The presence of a conserved family of G protein-coupled receptor kinases in vertebrates and invertebrates points to the central role of these kinases in signal transduction cascades.

PubMed Disclaimer

References

    1. Cell. 1990 May 18;61(4):635-45 - PubMed
    1. Annu Rev Neurosci. 1989;12:67-83 - PubMed
    1. Annu Rev Cell Biol. 1986;2:391-419 - PubMed
    1. J Biol Chem. 1985 Apr 10;260(7):3883-6 - PubMed
    1. Proc Natl Acad Sci U S A. 1986 May;83(9):2797-801 - PubMed

Publication types

MeSH terms