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:

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}}