aspartylglucosaminidase, partial [Homo sapiens]

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.

Aspartylglucosaminuria. [GeneReviews(®). 1993]
Aspartylglucosaminuria.
Goodspeed K, Chen X, Tchan M. GeneReviews(®). 1993-2024. 2024 Jan 18
The T99K variant of glycosylasparaginase shows a new structural mechanism of the genetic disease aspartylglucosaminuria. [Protein Sci. 2019]
The T99K variant of glycosylasparaginase shows a new structural mechanism of the genetic disease aspartylglucosaminuria.
Pande S, Guo HC. Protein Sci. 2019 Jun; 28(6):1013-1023. Epub 2019 Apr 9.
Biochemical and structural insights into an allelic variant causing the lysosomal storage disorder - aspartylglucosaminuria. [FEBS Lett. 2018]
Biochemical and structural insights into an allelic variant causing the lysosomal storage disorder - aspartylglucosaminuria.
Pande S, Bizilj W, Guo HC. FEBS Lett. 2018 Aug; 592(15):2550-2561. Epub 2018 Jul 23.

RefSeq genomic sequence
See the genomic reference sequence for the AGA gene (NG_011845.2).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the AGA gene.

aspartylglucosaminidase, isoform CRA_c [Homo sapiens]
aspartylglucosaminidase, isoform CRA_c [Homo sapiens]
gi|119625119|gb|EAX04714.1||gnl|WGS |hCP1887616

Protein
AGA, partial [Homo sapiens]
AGA, partial [Homo sapiens]
gi|49456391|emb|CAG46516.1|

Protein

Your browsing activity is empty.

Activity recording is turned off.

Protein