L-iduronidase

L-iduronidase
L-idu·ron·i·dase (i″du-ronґĭ-dās) [EC 3.2.1.76] an enzyme of the hydrolase class that catalyzes the hydrolysis of terminal desulfated α-L-iduronic acid residues of dermatan sulfate and heparan sulfate, a step in the degradation of these glycosaminoglycans. Deficiency of the enzyme, an autosomal recessive trait, leads to mucopolysaccharidosis I.

Medical dictionary. 2011.

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  • Iduronidase — Vorhandene Strukturdaten …   Deutsch Wikipedia

  • Iduronidase — protein Name = iduronidase, α L caption = width = HGNCid = 5391 Symbol = IDUA AltSymbols = EntrezGene = 3425 OMIM = 252800 RefSeq = NM 000203 UniProt = P35475 PDB = ECnumber = 3.2.1.76 Chromosome = 4 Arm = p Band = 16.3 LocusSupplementaryData =… …   Wikipedia

  • iduronidase — (= a 1 iduronidase) EC 3.2.1.76. An enzyme (653 amino acids in human) that hydrolyses the bonds between iduronic acid and N acetylgalactosamine 4 sulphate; a lysosomal enzyme absent in Hurler s disease …   Dictionary of molecular biology

  • Α-L-Iduronidase — Iduronidase Vorhandene Strukturdaten: 1Y24 …   Deutsch Wikipedia

  • α-l-iduronidase — An enzyme that hydrolyzes terminal desulfated α l iduronic acid residues of dermatan sulfate and of heparan sulfate; a deficiency of this enzyme is associated with Hurler syndrome and Scheie syndrome …   Medical dictionary

  • IDUA — Iduronidase Vorhandene Strukturdaten: 1Y24 …   Deutsch Wikipedia

  • Laronidase — Iduronidase Vorhandene Strukturdaten: 1Y24 …   Deutsch Wikipedia

  • IDUA — iduronidase …   Medical dictionary

  • IDUA — • iduronidase …   Dictionary of medical acronyms & abbreviations

  • Gargoylismus — Klassifikation nach ICD 10 E76 Störungen des Glykosaminoglykan Stoffwechsels Mukopolysaccharidose …   Deutsch Wikipedia

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