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Literature summary for 1.11.2.1 extracted from

  • Mireles, R.; Ramirez-Ramirez, J.; Alcalde, M.; Ayala, M.
    Ether oxidation by an evolved fungal heme-peroxygenase Insights into substrate recognition and reactivity (2021), J. Fungi (Basel), 7, 608 .
    View publication on PubMedView publication on EuropePMC

Inhibitors

Inhibitors Comment Organism Structure
benzyloxyacetate reversible inhibitor Cyclocybe aegerita
H2O2 the enzyme is quickly inactivated due to an excess of hydrogen peroxide Cyclocybe aegerita

Organism

Organism UniProt Comment Textmining
Cyclocybe aegerita B9W4V6
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonate) + H2O2
-
Cyclocybe aegerita oxidized 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonate) + H2O + H2O
-
?
2-(benzyloxy)ethanol + H2O2
-
Cyclocybe aegerita ? + H2O
-
?
5-nitro-1,3-benzodioxole + H2O2
-
Cyclocybe aegerita 4-nitrocatechol + H2O
-
?
allylbenzylether + H2O2 lowest turnover number Cyclocybe aegerita ? + H2O
-
?
benzyloxyacetaldehyde + H2O2 high turnover number Cyclocybe aegerita ? + H2O
-
?
dibenzylether + H2O2 highest turnover number Cyclocybe aegerita ? + H2O
-
?
additional information benzyloxyacetate is not a substrate Cyclocybe aegerita ?
-
-

Synonyms

Synonyms Comment Organism
PaDa-I
-
Cyclocybe aegerita
UPO
-
Cyclocybe aegerita

Cofactor

Cofactor Comment Organism Structure
heme
-
Cyclocybe aegerita

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
3.45
-
benzyloxyacetate at pH 7.0 and 30°C Cyclocybe aegerita