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AGA gene

Known as: ASPARTYLGLUCOSAMINIDASE, ASRG, GLYCOSYLASPARAGINASE 
National Institutes of Health

Related topics

Related topics

2 relations
AspartylglucosaminuriaAspartylglucosylaminase

Papers overview

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2004
2004
Identification of an aspartylglucosaminidase-like protein in the venom of the parasitic wasp Asobara tabida (Hymenoptera: Braconidae).
2004
2004
Autoproteolytic activation of human aspartylglucosaminidase.
Aspartylglucosaminidase (AGA) belongs to the N-terminal nucleophile (Ntn) hydrolase superfamily characterized by an N-terminal… 
1997
1997
Influence of L-fucose attached alpha 1-->6 to the asparagine-linked N-acetylglucosamine on the hydrolysis of the N-glycosidic linkage by human glycosylasparaginase.
The sequence of hydrolytic reactions in the catabolism of the N-glycosidic oligosaccharide-to-protein region containing 6-linked… 
1995
1995
Molecular cloning and sequence analysis of Flavobacterium meningosepticum glycosylasparaginase: a single gene encodes the alpha and beta subunits.
A full-length insert for the Flavobacterium meningosepticum N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase gene was located… 
1994
1994
The three-dimensional structure of PNGase F, a glycosylasparaginase from Flavobacterium meningosepticum.
BACKGROUND Peptide:N-glycosidase F (PNGase F) is an enzyme that catalyzes the complete removal of N-linked oligosaccharide chains… 
1993
1993
Post‐translational processing and Thr‐206 are required for glycosylasparaginase activity
1992
1992
Comparison of liver glycosylasparaginases from six vertebrates.
Structural and physical properties of glycosylasparaginase (EC 3.5.1.26) from the livers of human, pig, cow, rat, mouse and… 
1990
1990
Cloning and sequence analysis of a cDNA for human glycosylasparaginase
1990
1990
Cloning and sequence analysis of a cDNA for human glycosylasparaginase. A single gene encodes the subunits of this lysosomal amidase.
1989
1989
Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptides.
We have characterized the properties of human aspartylglucosaminidase (EC 3.5.1.26), the lysosomal enzyme which is deficient in… 
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