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Results 1 - 9 of 9
EC Number
Reaction
Commentary
Reference
1-(4-methoxyphenyl)-N-methyl-N-[(3-methyloxetan-3-yl)methyl]methanamine + H2O = 2-({[(4-methoxyphenyl)methyl](methyl)amino}methyl)-2-methylpropane-1,3-diol
(2)
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cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol
(1)
-
cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol
active site structure, quantitative structure-activity relationships, molecular modelling
cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol
formation of threo-1,2-diphenyl-1,2-ethanediols from all epoxides involving anti-stereospecific opening of the oxirane ring with about 90% preference for the (S)-carbon to give nearly optically pure (R,R)-diols
cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol
reaction mechanism, catalytic triad
cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol
the catalytic triad is Asp223-Glu402-His429, the active site includes an oxyanion hole
cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol
the catalytic triad is Asp226-His431-Asp352, catalytic mechanism involving an ester intermediate formed by alkylation of an active site carboxyl group
cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol
two step mechanism with formation of of a hydroxyl-alkyl-enzyme intermediate, catalytic triad
cis-stilbene oxide + H2O = (1R,2R)-1,2-diphenylethane-1,2-diol
two step mechanism with formation of of a hydroxyl-alkyl-enzyme intermediate, the catalytic triad is Asp226-His431-Glu404 with polarizing residues Tyr299 and Tyr374
Results 1 - 9 of 9