Identification of phosphorylation sites in the COOH-terminal tail of the μ-opioid receptor-Reference-Cited by-同舟云学术

Identification of phosphorylation sites in the COOH-terminal tail of the μ-opioid receptor

Published:2012-11-30 Issue:2 Volume:124 Page:189-199
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Chen Ying-Ju¹,Oldfield Sue¹,Butcher Adrian J.²,Tobin Andrew B.²,Saxena Kunal¹,Gurevich Vsevolod V.³,Benovic Jeffrey L.⁴,Henderson Graeme¹,Kelly Eamonn¹

Affiliation:

1. School of Physiology and Pharmacology; University of Bristol; Bristol UK

2. MRC Toxicology Unit; University of Leicester; Leicester UK

3. Department of Pharmacology; Vanderbilt University Medical Center Nashville; Nashville Tennessee USA

4. Department of Biochemistry and Molecular Biology; Thomas Jefferson University; Philadelphia Pennsylvania USA

Funder

Medical Research Council UK

NIH

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jnc.12071/fullpdf

Reference50 articles.

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3. Synthetic peptides of the hamster beta 2-adrenoceptor as substrates and inhibitors of the beta-adrenoceptor kinase;Benovic;Br. J. Clin. Pharmacol.,1990

4. Identification of serine 356 and serine 363 as the amino acids involved in etorphine-induced down-regulation of the μ-opioid receptor;Burd;J. Biol. Chem.,1998

5. Site-specific phosphorylation of CXCR4 is dynamically regulated by multiple kinases and results in differential modulation of CXCR4 signaling;Busillo;J. Biol. Chem.,2010

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