Protein Variants | Comment | Organism |
---|---|---|
V172L | the mutation leads to recessive congenital methaemoglobinaemia type I | Homo sapiens |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
NADH + ferricytochrome b5 | Homo sapiens | - |
NAD+ + H+ + ferrocytochrome b5 | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
NADH + ferricytochrome b5 | - |
Homo sapiens | NAD+ + H+ + ferrocytochrome b5 | - |
? |
Synonyms | Comment | Organism |
---|---|---|
cb5r | - |
Homo sapiens |
NADH-cytochrome b5 reductase | - |
Homo sapiens |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
FAD | - |
Homo sapiens |
General Information | Comment | Organism |
---|---|---|
malfunction | recessive congenital methaemoglobinaemia is caused by a deficiency of NADH-cytochrome b5 reductase | Homo sapiens |