Curated Information
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Home > Curated Information Page > PubMed Id: 27686097
Pangou E, et al. (2016) HIF-2α phosphorylation by CK1δ promotes erythropoietin secretion in liver cancer cells under hypoxia. J Cell Sci 129, 4213-4226 27686097
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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S383-p - HIF2A (human)
Modsite: SSGKGAVsEkSNFLF SwissProt Entrez-Gene
Orthologous residues
HIF2A (human): S383‑p, HIF2A (mouse): T383‑p, HIF2A (rat): S383‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mass spectrometry (in vitro), mutation of modification site
Disease tissue studied:  liver cancer, hepatocellular carcinoma
Relevant cell lines - cell types - tissues:  HepG2 (hepatic), Huh7 (hepatic)
Cellular systems studied:  cell lines
Species studied:  human
Enzymes shown to modify site in vitro
Type Enzyme
KINASE CK1D (human)
Downstream Regulation
Effect of modification (function):  intracellular localization
Effect of modification (process):  transcription, induced
Comments:  EPO secretion, inhibits CRM1-dependent nuclear export of HIF2A

T528-p - HIF2A (human)
Modsite: FNELDLEtLAPYIPM SwissProt Entrez-Gene
Orthologous residues
HIF2A (human): T528‑p, HIF2A (mouse): T527‑p, HIF2A (rat): T527‑p
Characterization
Methods used to characterize site in vivo immunoprecipitation, mass spectrometry (in vitro), mutation of modification site
Disease tissue studied:  liver cancer, hepatocellular carcinoma
Relevant cell lines - cell types - tissues:  HepG2 (hepatic), Huh7 (hepatic)
Cellular systems studied:  cell lines
Species studied:  human
Enzymes shown to modify site in vitro
Type Enzyme
KINASE CK1D (human)
Downstream Regulation
Effect of modification (function):  intracellular localization
Effect of modification (process):  transcription, induced
Comments:  EPO secretion, inhibits CRM1-dependent nuclear export of HIF2A