Abstract
The iron of the binuclear active center of [NiFe]-hydrogenases carries two CN and one CO ligands which are thought to confer to the metal a low oxidation and/or spin state essential for activity. Based on the observation that one of the seven auxiliary proteins required for the synthesis and insertion of the [NiFe] cluster contains a sequence motif characteristic of O-carbamoyl-transferases it was discovered that carbamoyl phosphate is essential for formation of active [NiFe]-hydrogenases in vivo and is specifically required for metal center synthesis suggesting that it is the source of the CO and CN ligands. A chemical path for conversion of a carbamoyl group into cyano and carbonyl moieties is postulated.
Original language | English (US) |
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Pages (from-to) | 9-12 |
Number of pages | 4 |
Journal | FEBS Letters |
Volume | 488 |
Issue number | 1-2 |
DOIs | |
State | Published - Jan 12 2001 |
Keywords
- Carbamoylphosphate
- Cyano/carbonyl ligand
- Metal center formation
- [NiFe]-Hydrogenase
ASJC Scopus subject areas
- Biophysics
- Structural Biology
- Biochemistry
- Molecular Biology
- Genetics
- Cell Biology