Curated Information
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Home > Curated Information Page > PubMed Id: 16563698
Hinchliffe KA, Irvine RF (2006) Regulation of type II PIP kinase by PKD phosphorylation. Cell Signal 18, 1906-13 16563698
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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T376-p - PIP4K2A (human)
Modsite: KAAHAAktVKHGAGA SwissProt Entrez-Gene
Orthologous residues
PIP4K2A (human): T376‑p, PIP4K2A (mouse): T376‑p, PIP4K2A (rat): T376‑p
Characterization
Methods used to characterize site in vivo 2D analysis, [32P] bio-synthetic labeling, mutation of modification site, phospho-antibody
Relevant cell lines - cell types - tissues:  HeLa (cervical), RAW 264 (macrophage)
Cellular systems studied:  cell lines
Species studied:  human, mouse
Enzymes shown to modify site in vitro
Type Enzyme
KINASE PRKD1 (human)
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE PRKD1 (human) activation of upstream enzyme, pharmacological inhibitor of upstream enzyme
Treatments, proteins and their effect on site modification: 
Treatments Referenced Treatments Manipulated Protein Referenced Protein Effect Notes
H2O2 increase
Go_6976 decrease
Downstream Regulation
Effect of modification (function):  enzymatic activity, inhibited

S910-p - PRKD1 (human)
Modsite: KALGERVsIL_____ SwissProt Entrez-Gene
Orthologous residues
PRKD1 (human): S910‑p, PRKD1 (mouse): S916‑p, PRKD1 (rat): S916‑p
Characterization
Methods used to characterize site in vivo phospho-antibody
Relevant cell lines - cell types - tissues:  HeLa (cervical), RAW 264 (macrophage)
Cellular systems studied:  cell lines
Species studied:  human, mouse
Upstream Regulation
Potential in vivo enzymes for site: 
Type Enzyme Evidence Notes
KINASE PRKD1 (human) activation of upstream enzyme
Downstream Regulation
Effect of modification (function):  enzymatic activity, induced