$VAR1 = undef;

Summary for peptidase T02.001: glycosylasparaginase precursor

Names
MEROPS Name	glycosylasparaginase precursor
Other names	aspartylglucosaminidase precursor, glycoasparaginase precursor

Domain architecture

MEROPS Classification
Classification	Clan PB >> Subclan PB(T) >> Family T2 >> Subfamily (none) >> T02.001
Holotype	glycosylasparaginase precursor (Homo sapiens), Uniprot accession P20933 (peptidase unit: 206-346), MERNUM MER0003299
History	Identifier created: MEROPS 3.4 (5 November 1999)

Activity
Catalytic type	Threonine
NC-IUBMB	Not yet included in IUBMB recommendations.
Activity status	human: active (Aronson, 2004) mouse: active (Kaartinen et al., 1998)
Knockout	A deficiency of glycosylasparaginase results in the human genetic disorder known as aspartylglycosaminuria (Oinonen et al., 1995). Mice with targeted disruption of the glycosylasparaginase gene may form a model for the human disease (Kaartinen et al., 1998).
Pathways	KEGG	Other glycan degradation
Other databases	TREEFAM	http://www.treefam.org/family/TF300756