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

BRENDA support

Literature summary extracted from

  • Rahier, A.; Taton, M.; Beneviste, P.
    Cycloeucalenol-obtusifoliol isomerase (1989), Eur. J. Biochem., 181, 615-626.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
5.5.1.9 3beta-Aminocycloeucalene 0.2 mM, weak Zea mays
5.5.1.9 4beta-Methylcycloeucalenol 0.2 mM, weak Zea mays
5.5.1.9 7-Keto-24,28-dihydrocycloeucalenol
-
Zea mays
5.5.1.9 7alpha-Hydroxy-24,28-dihydrocycloeucalenol
-
Zea mays
5.5.1.9 7beta-Hydroxy-24,28-dihydrocycloeucalenol
-
Zea mays
5.5.1.9 Cycloartenol 0.2 mM, weak Zea mays
5.5.1.9 Cycloeucalenyl 3beta-methyl ether 0.2 mM, weak Zea mays
5.5.1.9 DELTA6-24,28-Dihydrocycloeucalenol
-
Zea mays
5.5.1.9 DELTA7-24,28-Dihydrocycloeucalenol
-
Zea mays

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
5.5.1.9 0.1
-
cycloeucalenol
-
Zea mays

Organism

EC Number Organism UniProt Comment Textmining
5.5.1.9 Zea mays
-
-
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
5.5.1.9 embryo
-
Zea mays
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
5.5.1.9 cycloeucalenol
-
Zea mays obtusifoliol
-
?
5.5.1.9 additional information significant binding required the presence of the 3beta-hydroxyl group on the ring A with the correct stereochemistry together with absence of a 4beta-methyl group Zea mays ?
-
?