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Results 1 - 8 of 8

EC Number	Natural Substrates	Commentary (Nat. Sub.)
1.14.14.45	(E)-4-hydroxyphenylacetaldoxime + O2 + [reduced NADPH-hemoprotein reductase]	-
1.14.14.45	(E)-indol-3-ylacetaldehyde oxime + [reduced NADPH-hemoprotein reductase] + glutathione + O2	-
1.14.14.45	(E)-p-hydroxyphenylacetaldehyde oxime + [reduced NADPH-hemoprotein reductase] + glutathione + O2	-
1.14.14.45	(E)-phenylacetaldehyde oxime + [reduced NADPH-hemoprotein reductase] + glutathione + O2	-
1.14.14.45	1-aci-nitro-2-(4-hydroxyphenyl)-ethane + 2-mercaptoethanol	-
1.14.14.45	an (E)-omega-(methylthio)alkanal oxime + O2 + glutathione + [reduced NADPH-hemoprotein reductase]	-
1.14.14.45	indole-3-acetaldoxime + [reduced NADPH-hemoprotein reductase] + O2	-
1.14.14.45	more	CYP83B1 catalyzes the conversion of the (E)-p-hydroxyphenylacetaldoxime into an S-alkyl-thiohydroximate with retention of the configuration of the E-oxime intermediate in the final glucosinolate core structure. CYP83B1 from Arabidopsis thaliana cannot convert the (E)-p-hydroxyphenylacetaldoxime to the (Z)-isomer, which blocks the route towards cyanogenic glucoside synthesis

Results 1 - 8 of 8

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Release 2023.1 (January 2023)