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1 ence of the D(kcat/KNE) value with 1,1-[2H2]-nitroethane.
2 atalyze the formation of ethylnitronate from nitroethane.
3 um kinetic isotope effects with 1,2-[(2)H(4)]nitroethane and 1,1,2-[(2)H(3) ethyl nitronate at pH 8 y
5 oton transfer reaction between the substrate nitroethane and Asp-402 catalyzed by nitroalkane oxidase
6 5.5 +/- 0.3 s(-)(1) and the K(m) values for nitroethane and oxygen are 3.3 +/- 0.6 and 0.023 +/- 0.0
10 e second-order rate constant k cat/ K m with nitroethane as substrate implicates the presence of a gr
11 spora crassa 2-nitropropane dioxygenase with nitroethane as substrate occurs through both nonoxidativ
12 he kinetic isotope effects with [1,1-(2)H(2)]nitroethane as substrate was measured in the current stu
16 form of the enzyme has been determined with nitroethane at pH 7 to be bi-ter ping-pong, with oxygen
18 ldehyde are noncompetitive inhibitors versus nitroethane due to formation of a dead-end complex betwe
19 petitive inhibitor valerate, indicating that nitroethane has no significant external commitments to c
20 d kinetic isotope effects with [1, 1-(2)H(2)]nitroethane have been used to study the mechanism of thi
21 state kinetic mechanism with 2-nitropropane, nitroethane, nitrobutane, and nitrohexane, in either the
24 me inactivated by cyanide in the presence of nitroethane or nitrohexane shows that a flavin cyanoethy
26 med from the H196-catalyzed deprotonation of nitroethane partitions between release from the active s
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