Curated Information
Javascript is not enabled on this browser. This site will not work properly without Javascript.
PhosphoSitePlus Homepage PhosphoSitePlus® v6.8.2
Powered by Cell Signaling Technology
Home > Curated Information Page > PubMed Id: 19959593
Clayton CC, Bruchas MR, Lee ML, Chavkin C (2010) Phosphorylation of the mu-opioid receptor at tyrosine 166 (Tyr3.51) in the DRY motif reduces agonist efficacy. Mol Pharmacol 77, 339-47 19959593
This page summarizes selected information from the record referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2015, 43:D512-20). To learn more about the scope of PhosphoSitePlus®, click here.
Click on the protein name to open the protein page, and on the RSD number to open the site page.
Download

Y166-p - MOR-1 (rat)
Modsite: CTMSVDRyIAVCHPV SwissProt Entrez-Gene
Orthologous residues
MOR‑1 (human): Y168‑p, MOR‑1 iso5 (human): Y168‑p, MOR‑1 (mouse): Y166‑p, MOR‑1 (rat): Y166‑p
Characterization
Methods used to characterize site in vivo mutation of modification site, phospho-antibody, western blotting
Relevant cell lines - cell types - tissues:  293 (epithelial)
Cellular systems studied:  cell lines
Species studied:  human
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
DAMGO no change compared to control
H2O2 no change compared to control
H2O2, DAMGO increase
EGF no change compared to control
DAMGO, EGF increase
naloxone DAMGO, EGF inhibit treatment-induced increase
PP2 DAMGO, EGF inhibit treatment-induced increase
Downstream Regulation
Effect of modification (function):  activity, inhibited
Comments:  reduces G-protein coupling efficiency of the mu opioid receptor