
Cleavage by the GPI-PLD provides definitive evidence of a minimal GPI structure: glucosamine-phosphatidylinositol. Unlike the case for PI-PLC, cleavage by the GPI-PLD is unaffected by acylation of the inositol ring. Thus the GPI-PLD provides an excellent simple enzymatic tool for analyzing the basic core structure of GPI anchors.
Mammals, Glucosamine, DNA, Complementary, Cations, Divalent, Glycosylphosphatidylinositols, Acylation, Detergents, Gene Expression, Chromatography, Ion Exchange, Chromatography, Affinity, Kinetics, Carbohydrate Sequence, Carbohydrate Conformation, Chromatography, Gel, Escherichia coli, Animals, Humans, Cattle, Electrophoresis, Polyacrylamide Gel, Cloning, Molecular
Mammals, Glucosamine, DNA, Complementary, Cations, Divalent, Glycosylphosphatidylinositols, Acylation, Detergents, Gene Expression, Chromatography, Ion Exchange, Chromatography, Affinity, Kinetics, Carbohydrate Sequence, Carbohydrate Conformation, Chromatography, Gel, Escherichia coli, Animals, Humans, Cattle, Electrophoresis, Polyacrylamide Gel, Cloning, Molecular
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