Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 1.12.99.6 extracted from

  • Wright, J.A.; Pickett, C.J.
    Protonation of a subsite analogue of [FeFe]-hydrogenase: mechanism of a deceptively simple reaction revealed by time-resolved IR spectroscopy (2009), Chem. Commun. (Camb. ), 38, 5719-5721.
    View publication on PubMed

Metals/Ions

Metals/Ions Comment Organism Structure
Fe protonation can take place in a terminal fashion at a single Fe or by bridging between two iron centres, protonation of a model of the subsite of [FeFe]-hydrogenase, [Fe2(m-pdt)(CO)4(PMe3)2], occurs via a two-step mechanism synthetic construct

Organism

Organism UniProt Comment Textmining
synthetic construct
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information protonation of a model of the subsite of [FeFe]-hydrogenase, [Fe2(micro-pdt)(CO)4(PMe3)2]. The deceptively simple stoichiometric reaction is limited by the rate of protonation of the basal-apical isomer followed by its rearrangement to the transoid basal form synthetic construct ?
-
?

Synonyms

Synonyms Comment Organism
[FeFe] hydrogenase
-
synthetic construct

General Information

General Information Comment Organism
physiological function protonation is a fundamental step in hydrogen evolution at the di-iron subsite of [FeFe]-hydrogenase synthetic construct