Your IP: 18.205.176.85 United States Near: Cambridge, Massachusetts, United States

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aspartoacylase (Canavan disease) Identifiers Symbol ASPA Entrez 443 HUGO 756 OMIM 608034 RefSeq NM_000049 UniProt P45381 Other data EC number 3.5.1.15 Locus Chr. 17 p13-ter aspartoacylase (aminocyclase) 3 Identifiers Symbol ACY3 Entrez 91703 HUGO 24104 RefSeq NM_080658 UniProt Q96HD9 Other data Locus Chr. 11 q13 Aspartoacylase is a hydrolase enzyme which breaks down N-acetylaspartate. A deficiency is associated with Canavan disease. External links MeSH aspartoacylase This hydrolase article is a stub. You can help Wikipedia by expanding it. v • d • e v • d • e Hydrolases: carbon-nitrogen non-peptide (EC 3.5) 3.5.1: Linear amides / Amidohydrolases Asparaginase · Glutaminase · Urease · Biotinidase · Aspartoacylase · Ceramidase · Aspartylglucosaminidase · Fatty acid amide hydrolase · Histone deacetylase (Sirtuin) 3.5.2: Cyclic amides/ Amidohydrolases Barbiturase · Beta-lactamase 3.5.3: Linear amidines/ Ureohydrolases Arginase · Agmatinase · Protein-arginine deiminase 3.5.4: Cyclic amidines/ Aminohydrolases Guanine deaminase · Adenosine deaminase · AMP deaminase · Inosine monophosphate synthase · DCMP deaminase · GTP cyclohydrolase I 3.5.5: Nitriles/ Aminohydrolases Nitrilase 3.5.99: Other Riboflavinase · Thiaminase II