Journal of Computational Chemistry · 1992 · 21 citations · 12 references
Life SciencesBiochemistryMolecular BiologyBiophysical ChemistryEnzyme MechanismEnzymologyCatalytic MechanismsCatalytic Reaction KineticsEnzyme Active SitesEnzyme BiophysicsEnzyme KineticsKinetic ModelingBrownian DynamicsBrownian Dynamics ModelingBrownian Dynamics SimulationEnzyme Kinetic AnalysisEnzyme Kinetic ModelsEnzyme Reaction KineticsEnzyme-substrate Binding KineticsRate Constants
Abstract We used Brownian dynamics simulations of substrate O encounters with the enzyme bovine erythrocyte Cu, Zn superoxide dismutase (SOD) to study the effects of multiple charge modifications in the enzyme on the kinetics of its diffusion‐controlled reaction. When the charges of two or three residues were changed, the calculated rate consant relative to that for the unmodified enzyme was usually found to be the product of relative rate constants for the enzymes with the corresponding single‐site changes. This “multiplicativity” rule may be useful in the design of enzymes that operate with diffusion‐controlled kinetics. Residues that deviate from the general rule are found in the active site channel of SOD, and the origin of these deviations is considered.
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Brownian motion in a field of force and the diffusion model of chemical reactions
H. A. Kramers · Physica · 1940 · 8.6K citations
Natural Sciences, Chemistry, Physics +16
Oxygen and oxy‐radicals in chemistry and biology
Barry Halliwell · FEBS Letters · 1982 · 555 citations · Full text
Life Sciences, Biology, Chemistry +10
Electrostatic recognition between superoxide and copper, zinc superoxide dismutase
Elizabeth D. Getzoff, John A. Tainer, Paul K. Weiner et al. · Nature · 1983 · 555 citations