Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
endoplasmic reticulum | - |
Homo sapiens | 5783 | - |
Golgi apparatus | - |
Homo sapiens | 5794 | - |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | Q9C0D9 | - |
- |
Homo sapiens | Q9Y6K0 | cf. EC 2.7.8.2 | - |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
HEK-293 cell | - |
Homo sapiens | - |
Synonyms | Comment | Organism |
---|---|---|
CEPT1 | cf. EC 2.7.8.2 | Homo sapiens |
EPT1 | - |
Homo sapiens |
General Information | Comment | Organism |
---|---|---|
physiological function | CEPT1 is important for phosphatidylethanolamine formation from fatty acids such as 32:2, 32:1, 34:2, and 34:1. Brefeldin A treatment does not significantly affect the levels of the different phosphatidylethanolamine species. CEPT1 greatly prefers diacylglycerols 16:0-18:1 to other acceptors | Homo sapiens |
physiological function | EPT1 is important for the de novo biosynthesis of 1-alkenyl-2-acyl-glycerophosphoethanolamine. EPT1 also contributed to the synthesis of phosphatidylethanolamine species containing the fatty acids 36:1, 36:4, 38:5, 38:4, 38:3, 40:6, 40:5, and 40:4. EPT1 prefers 1-alkyl-2-acyl-glycerol 16-20:4 over 1,2-diacylglycerol 18:0-20:4 over 1,2-diacylglycerol 16:0-18:1 and 1-alkyl-2-acyl-glycerol 16-18:1 species as lipid acceptors | Homo sapiens |