Formimidoyltransferase cyclodeaminase
formimidoyltransferase cyclodeaminase | |||||||
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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 | ||||||
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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[edit]
Mutations of the FTCD gene cause glutamate formiminotransferase deficiency. [1]
See also[edit]
References[edit]
- ^ "Glutamate formiminotransferase deficiency". NIH. GARD. August 10, 2016. Retrieved December 21, 2020.
External links[edit]
- formiminotetrahydrofolate+cyclodeaminase at the U.S. National Library of Medicine Medical Subject Headings (MeSH)