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・ N-Acetyl Semax Amidate
・ N-acetyl-1-D-myo-inositol-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase
・ N-acetyl-beta-alanine deacetylase
・ N-acetyl-beta-glucosaminyl-glycoprotein 4-beta-N-acetylgalactosaminyltransferase
・ N-acetyl-D-glucosamine kinase
・ N-acetyl-gamma-glutamyl-phosphate reductase
・ N-acetyl-L-glutamate synthetase
・ N-Acetylanthranilic acid
・ N-Acetylaspartic acid
・ N-Acetylaspartylglutamic acid
・ N-acetyldiaminopimelate deacetylase
・ N-Acetylgalactosamine
・ N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase
・ N-acetylgalactosamine kinase
・ N-acetylgalactosamine-4-sulfatase
N-acetylgalactosamine-6-sulfatase
・ N-acetylgalactosamine-N,N'-diacetylbacillosaminyl-diphospho-undecaprenol 4-alpha-N-acetylgalactosaminyltransferase
・ N-acetylgalactosaminoglycan deacetylase
・ N-acetylgalactosaminyl-proteoglycan 3-beta-glucuronosyltransferase
・ N-Acetylglucosamine
・ N-acetylglucosamine deacetylase
・ N-acetylglucosamine kinase
・ N-Acetylglucosamine receptor
・ N-acetylglucosamine-1-phosphate transferase
・ N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
・ N-acetylglucosamine-6-phosphate deacetylase
・ N-acetylglucosamine-6-sulfatase
・ N-acetylglucosaminyl-diphospho-decaprenol L-rhamnosyltransferase
・ N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase
・ N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase


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N-acetylgalactosamine-6-sulfatase : ウィキペディア英語版
N-acetylgalactosamine-6-sulfatase

In enzymology, a N-acetylgalactosamine-6-sulfatase () is an enzyme that catalyzes the chemical reaction of cleaving off the 6-sulfate groups of the N-acetyl-D-galactosamine 6-sulfate units of the macromolecule chondroitin sulfate and, similarly, of the D-galactose 6-sulfate units of the macromolecule keratan sulfate.
This enzyme belongs to the family of hydrolases, specifically those acting on sulfuric ester bonds. The systematic name of this enzyme class is N-acetyl-D-galactosamine-6-sulfate 6-sulfohydrolase. Other names in common use include chondroitin sulfatase, chondroitinase, galactose-6-sulfate sulfatase, acetylgalactosamine 6-sulfatase, N-acetylgalactosamine-6-sulfate sulfatase, and N-acetylgalactosamine 6-sulfatase. This enzyme participates in glycosaminoglycan degradation and degradation of glycan structures.
==Deficiency==
Morquio syndrome is a rare birth defect caused by a deficiency in this essential enzyme. Treatment options include enzyme replacement therapy with a synthetic version of the enzyme called elosulfase alfa.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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