Glycosyl hydrolase family 59 | |||||||||
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Identifiers | |||||||||
Symbol | Glyco_hydro_59 | ||||||||
Pfam | PF02057 | ||||||||
Pfam clan | CL0058 | ||||||||
InterPro | IPR001286 | ||||||||
OPM superfamily | 117 | ||||||||
OPM protein | 3zr5 | ||||||||
CAZy | GH59 | ||||||||
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In molecular biology, glycoside hydrolase family 59 is a family of glycoside hydrolases.
Glycoside hydrolases EC 3.2.1. are a widespread group of enzymes that hydrolyse the glycosidic bond between two or more carbohydrates, or between a carbohydrate and a non-carbohydrate moiety. A classification system for glycoside hydrolases, based on sequence similarity, has led to the definition of >100 different families. [1] [2] [3] This classification is available on the CAZy web site, [4] [5] and also discussed at CAZypedia, an online encyclopedia of carbohydrate active enzymes. [6] [7]
Glycoside hydrolase family 59 CAZY GH_59 comprises enzymes with only one known activity; galactocerebrosidase (EC 3.2.1.46). Globoid cell leukodystrophy (Krabbe disease) is a severe, autosomal recessive disorder that results from deficiency of galactocerebrosidase (GALC) activity. [8] [9] [10] GALC is responsible for the lysosomal catabolism of certain galactolipids, including galactosylceramide and psychosine. [8]
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