1APY, 1APZ
175
11593
ENSG00000038002
ENSMUSG00000031521
P20933
Q64191
NM_000027NM_001171988
NM_001005847NM_001205054
NP_000018NP_001165459
NP_001005847NP_001191983
N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase is an enzyme that in humans is encoded by the AGA gene.[5]
Aspartylglucosaminidase is an amidohydrolase enzyme 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.[5]
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