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Results 1 - 9 of 9
EC Number Substrates Commentary Substrates Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.2271-phosphatidyl-1D-myo-inositol + 6-((N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-hexanoyl)-sphingosine - ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.2271-phosphatidyl-1D-myo-inositol + C6-N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)ceramide - ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.2271-phosphatidyl-1D-myo-inositol + hydroxy fatty acid-containing ceramide - hydroxy fatty acid-containing inositolphosphoylceramide - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.2271-phosphatidyl-1D-myo-inositol + N-[(2R,4E)-1-hydroxyoctadec-4-en-2-yl]octanamide - 1,2-diacyl-sn-glycerol + ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.2271-phosphatidyl-1D-myo-inositol + N-[6-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl]-D-erythro-sphingosine - ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.2271-phosphatidyl-1D-myo-inositol + nonhydroxy fatty acid-containing ceramide - nonhydroxy fatty acid-containing inositolphosphoylceramide - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.227L-alpha-phosphatidylinositol + C6-NBD-ceramide - ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.227more maximum product formation is observed at 1-phosphatidyl-1D-myo-inositol concentrations in excess of 600 microM ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 2.7.1.227more synthesis of ceramide derivatives built around a set of hydroxybutenyl amine cores, exploring variations in the sphingosine tail, N-acyl unit and the degree of hydroxylation. The C-3 hydroxyl group is not essential for turnover but it provides enhanced affinity. A long (C13) hydrocarbon ceramide tail is necessary for both high affinity and turnover. The N-acyl chain also contributes to affinity, analogues lacking the amide linkage function as competitive inhibitors in both enzyme and cell-based assays ? - ?
Results 1 - 9 of 9