aspartylglucosamine

aspartylglucosamine
as·par·tyl·glu·co·sa·mine (ə-spahr″təl-gloo-kōsґə-mēn) N-acetylglucosamine in N-glycosidic linkage with the amino group of asparagine; it is an intermediate in the degradation of glycoproteins and accumulates abnormally in aspartylglycosaminuria.

Medical dictionary. 2011.

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  • Aspartylglucosamine — chembox new ImageFile=Aspartylglucosamine.png ImageSize=200px IUPACName=(2 S ) 4 [(2 R ,3 R ,4 R ,5 S ,6 R ) 3 Acetamido 4,5 dihydroxy 6 (hydroxymethyl)oxan 2 yl] amino] 2 amino 4 oxobutanoic acid OtherNames= Section1=Chembox Identifiers… …   Wikipedia

  • Aspartylglucosaminuria — Infobox Disease Name = PAGENAME Caption = Aspartylglucosamine DiseasesDB = 952 ICD10 = ICD10|E|77|1|e|70 ICD9 = ICDO = OMIM = 208400 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Aspartylglucosaminuria (AGU), also called… …   Wikipedia

  • aspartylglucosaminuria — as·par·tyl·glu·co·sa·min·uria (ə spahr″təl gloo″kōs am″in uґre ə) a severe autosomal recessive lysosomal storage disease caused mutations in the AGA gene (locus: 4q32 q33), which encodes… …   Medical dictionary

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