Any feedback?
Literature summary extracted from
- Genetic modifiers of degeneration in the cathepsin D deficient Drosophila model for neuronal ceroid lipofuscinosis (2009), Neurobiol. Dis., 36, 488-493.
Organism
| EC Number | Organism | UniProt | Comment | Textmining |
|---|---|---|---|---|
| 3.4.23.5 | Drosophila melanogaster | - |
- |
- |
Source Tissue
| EC Number | Source Tissue | Comment | Organism | Textmining |
|---|
Synonyms
| EC Number | Synonyms | Comment | Organism |
|---|---|---|---|
| 3.4.23.5 | cathD | - |
Drosophila melanogaster |
General Information
| EC Number | General Information | Comment | Organism |
|---|---|---|---|
| 3.4.23.5 | malfunction | mutations in cathepsin D result in the most severe, congenital form of neuronal ceroid lipofuscinoses with progressive intracellular accumulation of autofluorescent storage material, modest neurodegeneration in the brain areas related to visual function, and a retinal degenerative phenotype | Drosophila melanogaster |
Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.
Release 2023.1 (January 2023)
Legal
Curated at
Member of
