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Results 1 - 10 of 10
EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
(6E)-8-hydroxygeraniol + 2 NADP+
-
(6E)-8-oxogeranial + 2 NADPH + 2 H+
-
r
(6E)-8-hydroxygeraniol + 2 NADP+
-
(6E)-8-oxogeranial + 2 NADPH + 2 H+
-
?
(6E)-8-hydroxygeraniol + 2 NADP+
10-hydroxygeraniol undergoes a reversible dehydrogenation to produce 8-oxogeraniol or 8-hydroxygeranial, which are oxidized further to give 8-oxogeranial, the direct precursor of iridodial
(6E)-8-oxogeranial + 2 NADPH + 2 H+
-
r
(6E)-8-hydroxygeraniol + 2 NADP+
oxidization at C1 and C8, depending on numbering of the molecule, GC-MS product analysis
(6E)-8-oxogeranial + 2 NADPH + 2 H+
-
?
(6E)-8-hydroxynerol + 2 NADP+
-
? + 2 NADPH + 2 H+
-
r
(6E)-8-hydroxynerol + 2 NADP+
-
? + 2 NADPH + 2 H+
-
?
(6E)-8-hydroxynerol + 2 NADP+
oxidization at C1 and C8, depending on numbering of the molecule, GC-MS product analysis
? + 2 NADPH + 2 H+
-
?
geraniol + 2 NADP+
-
? + 2 NADPH + 2 H+
-
r
more
various branched-chain allylic primary alcohols, such as nerol, geraniol, and 8-hydroxygeraniol, are substrates, but ethanol is inert. The enzyme is also active with farnesol, 3-methyl-2-buten1-ol, citronellol, 4-isopropylbenzyl alcohol, trans-2-heptenol, and trans-2-hexenol. The enzyme exclusively transfers the pro-R hydrogen of NADPH to neral. No activity with linalool, 2,6-dimethyl-octane, iridodial, 1-octanol, 1-heptanol, 1-pentanol, 3-methyl-3-buten-1-ol, trans-crotyl alcohol, isopulegol, and menthol
?
-
-
nerol + 2 NADP+
-
? + 2 NADPH + 2 H+
-
r
Results 1 - 10 of 10