Curated Information
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Home > Curated Information Page > PubMed Id: 11069302
O'Connor DS, et al. (2000) Regulation of apoptosis at cell division by p34cdc2 phosphorylation of survivin. Proc Natl Acad Sci U S A 97, 13103-7 11069302
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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T34-p - Survivin (human)
Modsite: FLEGCACtPERMAEA SwissProt Entrez-Gene
Orthologous residues
Survivin (human): T34‑p, Survivin iso2 (human): T34‑p, Survivin (mouse): T34‑p, Survivin iso2 (mouse): T34‑p, Survivin (rat): T34‑p
Characterization
Methods used to characterize site in vivo [32P] bio-synthetic labeling, mutation of modification site, phospho-antibody
Relevant cell lines - cell types - tissues:  HeLa (cervical), YUSAC2 (melanocyte)
Cellular systems studied:  cell lines
Species studied:  human
Enzymes shown to modify site in vitro
Type Enzyme
KINASE CDK1 (human)
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE CDK1 (human) transfection of inactive enzyme
Downstream Regulation
Effect of modification (function):  molecular association, regulation
Effect of modification (process):  apoptosis, inhibited
Modification regulates interactions with: 
Interacting molecule Interacting domains Effect Consequences (function) Consequences (process) Detection assays
CASP9 (human) Induces apoptosis, altered electrophoretic visualization, co-immunoprecipitation