Curated Information
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Home > Curated Information Page > PubMed Id: 11842186
Chen F, et al. (2002) Arsenite-induced Cdc25C degradation is through the KEN-box and ubiquitin-proteasome pathway. Proc Natl Acad Sci U S A 99, 1990-5 11842186
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.
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K151-ub - CDC25C (human)
Modsite: MCsSsANkENDNGNL SwissProt Entrez-Gene
Orthologous residues
CDC25C (human): K151‑ub, CDC25C iso3 (human): K108‑ub, CDC25C (mouse): K150‑ub, CDC25C (frog): K154‑ub
Characterization
Methods used to characterize site in vivo immunoprecipitation, modification-specific antibody, mutation of modification site, western blotting
Relevant cell lines - cell types - tissues:  BEAS-2B (epithelial)
Cellular systems studied:  cell lines
Species studied:  human
Upstream Regulation
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
arsenite, lactacystin increase
Downstream Regulation
Effect of modification (function):  protein degradation
Effect of modification (process):  cell cycle regulation, cell growth, inhibited