Formimidoyltransferase cyclodeaminase: Difference between revisions
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imported>CopperKettle →Role in pathology: Mutations of the FTCD gene cause glutamate formiminotransferase deficiency. |
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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]]. | '''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]]. | |||
==See also== | ==See also== | ||
Latest revision as of 08:40, 13 January 2019
| formimidoyltransferase cyclodeaminase | |
|---|---|
| Identifiers | |
| Symbol | FTCD |
| Entrez | 10841 |
| HUGO | 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.
See also
External links
- formiminotetrahydrofolate+cyclodeaminase at the US National Library of Medicine Medical Subject Headings (MeSH)
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