Application | Comment | Organism |
---|---|---|
medicine | short-chain-acyl-CoA-dehydrogenase deficiency is an inborn error of mitochondrial fatty acid metabolism caused by rare mutations as well as common susceptibility variations in the SCAD gene | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
butyryl-CoA + electron acceptor | - |
Homo sapiens | 2-butenoyl-CoA + reduced acceptor | - |
? |
Synonyms | Comment | Organism |
---|---|---|
SCAD | - |
Homo sapiens |
short-chain acyl-CoA dehydrogenase | - |
Homo sapiens |