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Results 1 - 9 of 9
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EC Number Reaction Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O - -
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O Asp402 acts as the active site base of the enzyme, mechanism, substrate CH-bond cleavage is rate limiting for the reduction of the enzyme by nitroethane 654710
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O Asp402 acts as the active site base of the enzyme, mechanism: catalysis is initiated by the active site base Asp402 that deprotonates the neutral substrate to yield a carbanion that can attack the N-5 position of the oxidized flavin, CH-bond cleavage is rate limiting for the reduction of the enzyme by nitroethane 655786
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O critical importance of the interaction between Asp402 and Arg409 for proton abstraction by nitroalkane oxidase 685114
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O detailed mechanism, with carbanion reaction intermediate formation, an aspartate residue is the active site base, substrate CH-bond cleavage is rate limiting for the reduction of the enzyme by nitroethane, the active site of the enzyme is a hydrophobic channel, tunneling, overview 654373
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O mechanism 639229
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O mechanism, involves removal of a proton from the nitroalkane, forming a carbanion which adds to the N5 of the flavin, elimination of nitrite from the resulting adduct forms an electrophilic imine intermediate which can be attacked by hydroxide 655799
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O mechanism, transition-state stabilization is essential, protein-substrate interactions in the transition state, reaction involves quantum mechaniscal tunneling, Asp402 is involved in initial abstraction of a proton from the neutral substrate, overview 655793
Display the word mapDisplay the reaction diagram Show all sequences 1.7.3.1ethylnitronate + O2 + FMNH2 = acetaldehyde + nitrite + FMN + H2O ping pong kinetic mechanism 639228
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