AGA Products

Description

Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme. [provided by RefSeq]

Bioinformatics

Entrez	175 Human
Uniprot	AAH12392 Human NP_001165459 Human P20933 Human
Product By Gene ID	175
Alternate Names	AGU Aspartylglucosaminidase aspartylglucosaminidase aspartylglucosylamine deaspartylase ASRG EC 3.5.1 EC 3.5.1.26 GA glycosylasparaginase Glycosylasparaginase N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase