| aspartic endopeptidase |
[EC 3.4.23] any member of the group of endopeptidases that have an acidic residue involved in the catalytic process and so have a pH optimum below 5.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| aspartyl |
the acyl radical of aspartic acid.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| aspartylglucosamine |
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.
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| aspartylglucosaminidase |
a lysosomal enzyme of the hydrolase class that catalyzes the cleavage of N-glycosidic linkages between N-acetylglucosamine and asparagine in glycoproteins, a step in the degradation of glycoproteins. Deficiency of the enzyme, an autosomal recessive trait, causes aspartylglycosaminuria. In EC nomenclature, called N4-β-N-acetylglucosaminyl-L--asparaginase.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| aspartylglucosaminuria |
aspartylglycosaminuria.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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