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Literature summary for 2.7.1.107 extracted from

  • Franks, C.E.; Campbell, S.T.; Purow, B.W.; Harris, T.E.; Hsu, K.L.
    The ligand binding landscape of diacylglycerol kinases (2017), Cell Chem. Biol., 24, 870-880.e5 .
    View publication on PubMedView publication on EuropePMC

Inhibitors

Inhibitors Comment Organism Structure
4-[bis(4-fluorophenyl)methylidene]piperidine
-
Homo sapiens
additional information isoform DGKalpha is not inhibited by ketanserin Homo sapiens
ritanserin inhibitor of isoform DGKalpha Homo sapiens

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ 50 mM used in assay conditions Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens P23743
-
-

Source Tissue

Source Tissue Comment Organism Textmining
HEK-293T cell
-
Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
ATP + 1,2-dioleoyl-sn-glycerol
-
Homo sapiens ADP + 1,2-dioleoyl-sn-glycerol 3-phosphate
-
?

Subunits

Subunits Comment Organism
? x * 80000, isoform DGKalpha, SDS-PAGE Homo sapiens

Synonyms

Synonyms Comment Organism
DGKA isoform Homo sapiens
DGKalpha isoform Homo sapiens
diacylglycerol kinase alpha isoform Homo sapiens

IC50 Value

IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
0.025
-
isoform DGKalpha, pH and temperature not specified in the publication Homo sapiens ritanserin
0.223
-
isoform DGKalpha, pH and temperature not specified in the publication Homo sapiens 4-[bis(4-fluorophenyl)methylidene]piperidine