Curated Information
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Curated Information Page
PubMed Id: 15326477 
Casanovas O, et al. (2004) P38SAPK2 phosphorylates cyclin D3 at Thr-283 and targets it for proteasomal degradation. Oncogene 23, 7537-44 15326477
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.
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T283-p - CCND3 (human)
Orthologous residues
CCND3 (human): T283‑p, CCND3 iso2 (human): T202‑p, CCND3 iso3 (human): T211‑p, CCND3 iso4 (human): T87‑p, CCND3 (mouse): T283‑p, CCND3 (rat): T284‑p
 Methods used to characterize site in vivo mutation of modification site
 Relevant cell lines - cell types - tissues:  COS (fibroblast), Jurkat (T lymphocyte), MOLT-4 (T lymphocyte)
 Cellular systems studied:  cell lines
 Species studied:  human, monkey
 Enzymes shown to modify site in vitro
Type Enzyme
KINASE P38B (human)
KINASE P38D (human)
KINASE P38G (human)
Downstream Regulation
 Effect of modification (function):  protein degradation

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