Formimidoyltransferase cyclodeaminase
{{Short description|Class of enzymes}}
{{Redirect|FTCD}}
{{protein
| Name = formimidoyltransferase cyclodeaminase
| AltNames = formiminotransferase cyclodeaminase
| caption = Formiminotransferase cyclodeaminase homooctamer, Rattus norvegicus
| image = 2pfd.jpg
| width = 270
| HGNCid = 3974
| Symbol = FTCD
| AltSymbols =
| EntrezGene = 10841
| OMIM = 606806
| RefSeq = NM_006657
| UniProt = O95954
| PDB =
| ECnumber =
| Chromosome = 21
| Arm = q
| Band = 22.3
| LocusSupplementaryData =
}}
Formimidoyltransferase cyclodeaminase or formiminotransferase cyclodeaminase (gene symbol FTCD in humans) is a bifunctional enzyme that catalyzes the following reactions:
- conversion of formiminoglutamate and tetrahydrofolate into formiminotetrahydrofolate and glutamate (glutamate formimidoyltransferase activity, {{EC number|2.1.2.5}})
- subsequent deamination of formiminotetrahydrofolate to 5,10-methenyltetrahydrofolate and ammonia (formimidoyltetrahydrofolate cyclodeaminase activity, {{EC number|4.3.1.4}})
Its name comes from the two activities it catalyzes.
Role in pathology
Mutations of the FTCD gene cause glutamate formiminotransferase deficiency.{{cite web |url=https://rarediseases.info.nih.gov/diseases/9279/glutamate-formiminotransferase-deficiency |title= Glutamate formiminotransferase deficiency
|author= |date=August 10, 2016 |website=NIH |publisher=GARD |access-date= December 21, 2020 |quote=}}
See also
References
{{Reflist}}{{lyase-stub}}{{Carbon-nitrogen lyases}}
{{Amino acid metabolism enzymes}}