Curated Information
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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.
Information from this record has been curated, but not yet edited in PhosphoSitePlus® and may be incomplete.
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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
Characterization
 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) pharmacological activator of upstream enzyme, phospho-antibody
KINASE PKCG (human) pharmacological activator of upstream enzyme, co-immunoprecipitation, phospho-antibody, transfection of wild-type enzyme, mutation in upstream enzyme recognition motif
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
phorbol ester increase
forskolin increase


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