Curated Information
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Home > Curated Information Page > PubMed Id: 24312625
Godin-Heymann N, Wang Y, Slee E, Lu X (2013) Phosphorylation of ASPP2 by RAS/MAPK Pathway Is Critical for Its Full Pro-Apoptotic Function. PLoS One 8, e82022 24312625
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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S827-p - 53BP2 (human)
Modsite: NSDMPAPsPGLDYEP SwissProt Entrez-Gene
Orthologous residues
53BP2 (human): S827‑p, 53BP2 iso3 (human): S833‑p, 53BP2 (mouse): S827‑p, 53BP2 (rat): P827‑p, 53BP2 (cow): S833‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mass spectrometry (in vitro), mutation of modification site, western blotting
Disease tissue studied:  bone cancer
Relevant cell lines - cell types - tissues:  Saos-2 (bone cell)
Cellular systems studied:  cell lines
Species studied:  human
Enzymes shown to modify site in vitro
Type Enzyme
KINASE ERK2 (human)
Downstream Regulation
Effect of modification (function):  intracellular localization
Effect of modification (process):  apoptosis, induced, transcription, induced
Comments:  necessary for Ras-induced translocation to the cytosol and nucleus, p53 mediated transcription and pro-apoptotic activity