Curated Information
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Curated Information Page
PubMed Id: 14988727 
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.
Li Y, et al. (2004) SPAK kinase is a substrate and target of PKCtheta in T-cell receptor-induced AP-1 activation pathway. EMBO J 23, 1112-22 14988727
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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S309-p - STLK3 (human)
Orthologous residues
STLK3 (human): S309‑p, STLK3 (mouse): S321‑p, STLK3 (rat): S318‑p
Characterization
 Methods used to characterize site in vivo mutation of modification site
 Relevant cell lines - cell types - tissues:  293T (epithelial)
 Cellular systems studied:  cell lines
 Species studied:  human
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE PKCT (human)
Downstream Regulation
 Effect of modification (function):  enzymatic activity, induced

S323-p - STLK3 (human)
Orthologous residues
STLK3 (human): S323‑p, STLK3 (mouse): S335‑p, STLK3 (rat): S332‑p
Characterization
 Methods used to characterize site in vivo mutation of modification site
 Relevant cell lines - cell types - tissues:  293T (epithelial)
 Cellular systems studied:  cell lines
 Species studied:  human
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE PKCT (human)
Downstream Regulation
 Effect of modification (function):  enzymatic activity, induced


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