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Literature summary extracted from
- A novel aspartoacylase (ASPA) gene mutation in Canavan disease (2012), Fetal. Pediatr. Pathol., 31, 236-239.
Protein Variants
| EC Number | Protein Variants | Comment | Organism |
|---|---|---|---|
| 3.5.1.15 | Y88X | the mutation is associated with Canavan disease | Homo sapiens |
Natural Substrates/ Products (Substrates)
| EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 3.5.1.15 | N-acetyl-L-aspartate + H2O | Homo sapiens | - |
L-aspartate + acetate | - |
? |  |
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 3.5.1.15 | Homo sapiens | - |
- |
- |
Source Tissue
| EC Number | Source Tissue | Comment | Organism | Textmining |
|---|---|---|---|---|
| 3.5.1.15 | fetus | - |
Homo sapiens | - |
Substrates and Products (Substrate)
| EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|---|
| 3.5.1.15 | N-acetyl-L-aspartate + H2O | - |
Homo sapiens | L-aspartate + acetate | - |
? | |
Synonyms
| EC Number | Synonyms | Comment | Organism |
|---|---|---|---|
| 3.5.1.15 | ASPA | - |
Homo sapiens |
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Release 2023.1 (January 2023)
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