Curated Information
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Curated Information Page
PubMed Id: 10961885 
This page summarizes selected information from the article 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.
Visconti R, et al. (2000) Importance of the MKK6/p38 pathway for interleukin-12-induced STAT4 serine phosphorylation and transcriptional activity. Blood 96, 1844-52 10961885
Only sites from this record are displayed on this page. Click on the protein name to open the protein page, and on the RSD number to open the site page. For the complete dataset, click the download button, on the right.
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Y694-p - STAT4 (mouse)
Orthologous residues
STAT4 (human): Y693‑p, STAT4 (mouse): Y694‑p, STAT4 (rat): Y693‑p
Upstream Regulation
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
IL-12 increase
Downstream Regulation
 Effect of modification (function):  activity, induced

S722-p - STAT4 (mouse)
Orthologous residues
STAT4 (human): S721‑p, STAT4 (mouse): S722‑p, STAT4 (rat): S721‑p
Characterization
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE P38A (mouse)
Upstream Regulation
 Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE P38A (mouse)
 Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
IL-12 increase
Downstream Regulation
 Effect of modification (function):  activity, induced


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