Literature summary for 3.5.1.26 extracted from

Mills, K.; Mills, P.; Jackson, M.; Worthington, V.; Beesley, C.; Mann, A.; Clayton, P.; Grunewald, S.; Keir, G.; Young, L.; Langridge, J.; Mian, N.; Winchester, B.
Diagnosis of congenital disorders of glycosylation type-I using protein chip technology (2006), Proteomics, 6, 2295-2304.

Search for more literature for 3.5.1.26

Application

Application	Comment	Organism
diagnostics	marker for the diagnosis of glycosylation type I (CDG-I)	Homo sapiens

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	-	-	-

Substrates and Products (Substrate)

Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
L-aspartic acid-b-7-amido-4-methylcoumarin + H2O	-	Homo sapiens	7-amino-4-methylcoumarin + L-aspartate	-	?

Synonyms

Synonyms	Comment	Organism
aspartylglucosaminidase	-	Homo sapiens

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Release 2023.1 (January 2023)