Protein Variants | Comment | Organism |
---|---|---|
L237P | the mutation is associated with congenital erythropoietic porphyria | Homo sapiens |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
hydroxymethylbilane | Homo sapiens | - |
uroporphyrinogen III + H2O | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | P10746 | - |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
lymphocyte | - |
Homo sapiens | - |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
hydroxymethylbilane | - |
Homo sapiens | uroporphyrinogen III + H2O | - |
? |
Synonyms | Comment | Organism |
---|---|---|
Uroporphyrinogen III cosynthase | - |
Homo sapiens |
General Information | Comment | Organism |
---|---|---|
malfunction | congenital erythropoietic porphyria is the rarest autosomal recessive porphyria resulting from a deficiency of uroporphyrinogen III cosynthase | Homo sapiens |