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・ Glycoside hydrolase family 15
・ Glycoside hydrolase family 16
・ Glycoside hydrolase family 17
・ Glycoside hydrolase family 18
・ Glycoside hydrolase family 19
・ Glycoside hydrolase family 2
・ Glycoside hydrolase family 20
・ Glycoside hydrolase family 22
・ Glycoside hydrolase family 24
・ Glycoside hydrolase family 25
・ Glycoside hydrolase family 26
・ Glycoside hydrolase family 27
・ Glycoside hydrolase family 28
・ Glycoside hydrolase family 29
・ Glycoside hydrolase family 3
Glycoside hydrolase family 30
・ Glycoside hydrolase family 31
・ Glycoside hydrolase family 32
・ Glycoside hydrolase family 33
・ Glycoside hydrolase family 34
・ Glycoside hydrolase family 35
・ Glycoside hydrolase family 36
・ Glycoside hydrolase family 37
・ Glycoside hydrolase family 38
・ Glycoside hydrolase family 39
・ Glycoside hydrolase family 4
・ Glycoside hydrolase family 42
・ Glycoside hydrolase family 43
・ Glycoside hydrolase family 44
・ Glycoside hydrolase family 45


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Glycoside hydrolase family 30 : ウィキペディア英語版
Glycoside hydrolase family 30

In molecular biology, glycoside hydrolase family 30 is a family of glycoside hydrolases.
Glycoside hydrolases 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.〔(Bairoch, A. "Classification of glycosyl hydrolase families and index of glycosyl hydrolase entries in SWISS-PROT". 1999. )〕 This classification is available on the CAZy(http://www.cazy.org/GH1.html) web site,〔(Henrissat, B. and Coutinho P.M. "Carbohydrate-Active Enzymes server". 1999. )〕 and also discussed at CAZypedia, an online encyclopedia of carbohydrate active enzymes.〔(CAZypedia, an online encyclopedia of carbohydrate-active enzymes. )〕
Glycoside hydrolase family 30 (CAZY GH_30 ) includes the mammalian glucosylceramidases. Human acid beta-glucosidase (D-glucosyl-N-acylsphingosine glucohydrolase), cleaves the glucosidic bonds of glucosylceramide and synthetic beta-glucosides. Any one of over 50 different mutations in the gene of glucocerebrosidase have been found to affect activity of this hydrolase, producing variants of Gaucher disease, the most prevalent lysosomal storage disease.〔
==References==


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