Javascript is not enabled on this browser. This site will not work properly without Javascript.
PhosphoSitePlus Homepage PhosphoSitePlus® v6.7.4
Powered by Cell Signaling Technology
Home > Curated Information Page > PubMed Id: 26008897
Thompson BJ, et al. (2015) DYRK1A controls the transition from proliferation to quiescence during lymphoid development by destabilizing Cyclin D3. J Exp Med 212, 953-70 26008897
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, 2015, 43:D512-20). To learn more about the scope of PhosphoSitePlus®, click here.
Click on the protein name to open the protein page, and on the RSD number to open the site page.
Download

T283-p - CCND3 (mouse)
Modsite: QGPSQTStPTDVTAI SwissProt Entrez-Gene
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
Characterization
Methods used to characterize site in vivo flow cytometry, mutation of modification site, western blotting
Relevant cell lines - cell types - tissues:  B lymphocyte, thymocyte
Cellular systems studied:  primary cells
Species studied:  mouse
Enzymes shown to modify site in vitro
Type Enzyme
KINASE DYRK1A (human)
Downstream Regulation
Effect of modification (function):  protein degradation
Effect of modification (process):  cell cycle regulation, cell differentiation, induced, transcription, inhibited