Formimidoyltransferase cyclodeaminase
(Redirected from Formiminotransferase cyclodeaminase)
| formimidoyltransferase cyclodeaminase | |||||||
|---|---|---|---|---|---|---|---|
 Formiminotransferase cyclodeaminase homooctamer, Rattus norvegicus | |||||||
| Identifiers | |||||||
| Symbol | FTCD | ||||||
| Alt. names | formiminotransferase cyclodeaminase | ||||||
| NCBI gene | 10841 | ||||||
| HGNC | 3974 | ||||||
| OMIM | 606806 | ||||||
| RefSeq | NM_006657 | ||||||
| UniProt | O95954 | ||||||
| Other data | |||||||
| EC number | 4.3.1.4 | ||||||
| Locus | Chr. 21 q22.3 | ||||||
| |||||||
Formimidoyltransferase cyclodeaminase or formiminotransferase cyclodeaminase (symbol FTCD in humans) is an enzyme that catalyzes the conversion of formiminoglutamate and tetrahydrofolate into formiminotetrahydrofolate and glutamate.
Role in pathology
Mutations of the FTCD gene cause glutamate formiminotransferase deficiency. [1]
See also
References
- ^ "Glutamate formiminotransferase deficiency". NIH. GARD. August 10, 2016. Retrieved December 21, 2020.
External links
- formiminotetrahydrofolate+cyclodeaminase at the U.S. National Library of Medicine Medical Subject Headings (MeSH)