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Ligand L-dihomomethionine Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
Basic Ligand Information Molecular Structure
C7 H1 5 NO2 S
L-dihomomethionine
FBWIRBFZWNIGJC-LURJTMIESA-N
Roles as Enzyme Ligand
In Vivo Substrate in Enzyme-catalyzed Reactions (2 results)
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L-dihomomethionine + 2 O2 + 2 [reduced NADPH-hemoprotein reductase] = 4-methylthiopentanaldoxime + CO2 + 3 H2O + 2 [oxidized NADPH-hemoprotein reductase]
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L-dihomomethionine + 2 O2 + 2 [reduced NADPH-hemoprotein reductase] = omega-(methylthio)-(E)-pentanaldehyde oxime + CO2 + 3 H2O + 2 [oxidized NADPH-hemoprotein reductase]
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Substrate in Enzyme-catalyzed Reactions (2 results)
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L-dihomomethionine + 2 O2 + 2 [reduced NADPH-hemoprotein reductase] = 4-methylthiopentanaldoxime + CO2 + 3 H2O + 2 [oxidized NADPH-hemoprotein reductase]
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L-dihomomethionine + 2 O2 + 2 [reduced NADPH-hemoprotein reductase] = omega-(methylthio)-(E)-pentanaldehyde oxime + CO2 + 3 H2O + 2 [oxidized NADPH-hemoprotein reductase]
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Enzyme Kinetic Parameters
KM Value (1 result)
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References & Links Literature References (2)
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Cytochrome p450 CYP79F1 from Arabidopsis catalyzes the conversion of dihomomethionine and trihomomethionine to the corresponding aldoximes in the biosynthesis of aliphatic glucosinolates
2001
Hansen, C.H.; Wittstock, U.; Olsen, C.E.; Hick, A.J.; Pickett, J.A.; Halkier, B.A.
J. Biol. Chem.
276
11078-11085
CYP79F1 and CYP79F2 have distinct functions in the biosynthesis of aliphatic glucosinolates in Arabidopsis
2003
Chen, S.; Glawischnig, E.; Jörgensen, K.; Naur, P.; Jörgensen, B.; Olsen, C.E.; Hansen, C.H.; Rasmussen, H.; Pickett, J.A.; Halkier, B.A.
Plant J.
33
923-937
Links to other databases for L-dihomomethionine