<p>NADP<sup>+</sup>-dependent activity (black circles) and activity with NAD<sup>+</sup> (white circles) was measured at nearly saturating co-substrate concentrations (bottom right corner). The data was fitted to the Michaelis-Menten equation and the Pearson correlation coefficient is indicated. The values for the kinetic parameters are given in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152403#pone.0152403.t001" target="_blank">Table 1</a>.</p
<p>Specific activity is shown in Units per mg of enzyme (U mg<sup>-1</sup>). U = μmol of NADH oxidiz...
<p>(A) Wild-type bglTm. (B) Mutant T1. (C) Mutant T2. The tested substrates were <i>p</i>-nitropheny...
<p>(A and B) are percentages of depletion of 20μM deltamethrin and permethrin by CYP6P9b mutants, re...
<p>NADP<sup>+</sup>-dependent activity (black circles) and activity with NAD<sup>+</sup> (white circ...
<p>Enzyme activity was determined at a fixed concentration of IMP (1 mM for IMPDHbt and 2 mM for IMP...
Enzyme kinetic parameters for rate equations are vital in metabolic network simulation, a major part...
<p>Enzyme activity was determined at a fixed concentration of NAD (2 mM for IMPDHbt and 6 mM for IMP...
Glucose-6-phosphate dehydrogenase (G6PD) catalyzes cellular biochemical oxidation-reduction reaction...
a<p>In all cases except for the cooperative model with the mutant S35A, k<sub>obs</sub> and K corres...
Glucose-6-phosphate dehydrogenase (G6PD) oxidizes glucose-6- phosphate (G6P) to 6-phosphoglucono-d-l...
In Escherichia coli, the pentose phosphate pathway is one of the main sources of NADPH. The first en...
Glucose-6-Phosphate dehydrogenase (G6PD) catalyzes cellular biochemical oxidation-reduction reaction...
<p>Data represent means ± SEM of 3 separate enzyme expressions each tested in duplicate. Note that t...
<p>All enzymes showed Michaelis-Menten kinetics with the tolerated amino acid substrates. The V<sub>...
Glucose-6-Phosphate Dehydrogenase (G6PD) catalyzes the first step in the Pentose Phosphate Pathway b...
<p>Specific activity is shown in Units per mg of enzyme (U mg<sup>-1</sup>). U = μmol of NADH oxidiz...
<p>(A) Wild-type bglTm. (B) Mutant T1. (C) Mutant T2. The tested substrates were <i>p</i>-nitropheny...
<p>(A and B) are percentages of depletion of 20μM deltamethrin and permethrin by CYP6P9b mutants, re...
<p>NADP<sup>+</sup>-dependent activity (black circles) and activity with NAD<sup>+</sup> (white circ...
<p>Enzyme activity was determined at a fixed concentration of IMP (1 mM for IMPDHbt and 2 mM for IMP...
Enzyme kinetic parameters for rate equations are vital in metabolic network simulation, a major part...
<p>Enzyme activity was determined at a fixed concentration of NAD (2 mM for IMPDHbt and 6 mM for IMP...
Glucose-6-phosphate dehydrogenase (G6PD) catalyzes cellular biochemical oxidation-reduction reaction...
a<p>In all cases except for the cooperative model with the mutant S35A, k<sub>obs</sub> and K corres...
Glucose-6-phosphate dehydrogenase (G6PD) oxidizes glucose-6- phosphate (G6P) to 6-phosphoglucono-d-l...
In Escherichia coli, the pentose phosphate pathway is one of the main sources of NADPH. The first en...
Glucose-6-Phosphate dehydrogenase (G6PD) catalyzes cellular biochemical oxidation-reduction reaction...
<p>Data represent means ± SEM of 3 separate enzyme expressions each tested in duplicate. Note that t...
<p>All enzymes showed Michaelis-Menten kinetics with the tolerated amino acid substrates. The V<sub>...
Glucose-6-Phosphate Dehydrogenase (G6PD) catalyzes the first step in the Pentose Phosphate Pathway b...
<p>Specific activity is shown in Units per mg of enzyme (U mg<sup>-1</sup>). U = μmol of NADH oxidiz...
<p>(A) Wild-type bglTm. (B) Mutant T1. (C) Mutant T2. The tested substrates were <i>p</i>-nitropheny...
<p>(A and B) are percentages of depletion of 20μM deltamethrin and permethrin by CYP6P9b mutants, re...