Curated Information
Javascript is not enabled on this browser. This site will not work properly without Javascript.
PhosphoSitePlus Homepage Cell Signaling Technology
HomeAbout PhosphoSiteUsing PhosphoSiteCuration ProcessContact
NIH-logos NIGMS Logo NIAAA Logo NCI Logo NIH Logo
Curated Information Page
PubMed Id: 17233759 
Gomes AR, et al. (2007) PKC anchoring to GluR4 AMPA receptor subunit modulates PKC-driven receptor phosphorylation and surface expression. Traffic 8, 259-69 17233759
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, 2012,40:D261-70). To learn more about the scope of PhosphoSitePlus®, click here.
Download Sites

S862-p - GluR4 (rat)
Orthologous residues
GluR4 (human): S862‑p, GluR4 iso2 (human): , GluR4 iso4 (human): , GluR4 (mouse): S862‑p, GluR4 iso2 (mouse): S862‑p, GluR4 (rat): S862‑p
 Methods used to characterize site in vivo phospho-antibody, western blotting
 Relevant cell lines - cell types - tissues:  'brain, hippocampus', 293 (epithelial), retina
 Cellular systems studied:  cell lines, primary cells, tissue
 Species studied:  chicken, human, rat
Upstream Regulation
 Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE PKACA (human) phospho-antibody, pharmacological activator of upstream enzyme
KINASE PKCG (human) mutation in upstream enzyme recognition motif, transfection of wild-type enzyme, phospho-antibody, co-immunoprecipitation, pharmacological activator of upstream enzyme
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
phorbol ester increase
forskolin increase

Home  |  Curator Login With enhanced literature mining using Linguamatics I2E I2E Logo Produced by 3rd Millennium  |  Design by Digizyme
©2003-2013 Cell Signaling Technology, Inc.