Biochemical Journal · 1972 · 147 citations · 20 references
Life SciencesBiochemistryMolecular BiologyCarbohydrate BiochemistryCarbohydrate ChemistryEnzymologyEnzyme InhibitionEnzyme KineticsSubstrate Specificity2'-O-methyl ModificationChemical ModificationSubstrate Binding AffinitySubstrate Binding SitesSubstrate Binding SpecificityYeast-substrate Interactionsβ-Glucosidase Activity
1. 2-Deoxy-2-fluoro-d-glucose, 2-deoxy-2-fluoro-d-mannose and 2-deoxy-2,2-difluoro-d-arabino-hexose are good substrates for yeast hexokinase. 2. 3-Deoxy-3-fluoro-d-glucose and 4-deoxy-4-fluoro-d-glucose are poor substrates and have very similar K(m) values (8x10(-2)m). 3. Neither alpha- nor beta-d-glucopyranosyl fluoride is a substrate or inhibitor. 4. Studies with 2-chloro-2-deoxy- and 2-O-methyl derivatives of d-glucose and d-mannose have revealed that little chemical modification is possible at position 2 without substantial loss in substrate binding. 5. The variation in the value of K(m) for the d-hexose derivatives was associated with a corresponding change in the value of K(m) for MgATP(2-) showing that the binding of MgATP(2-) is modified by the binding of the sugar.
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Statistical estimations in enzyme kinetics
GN WILKINSON · Biochemical Journal · 1961 · 3.6K citations · Full text
Computer Programmes for Processing Enzyme Kinetic Data
W. W. Cleland · Nature · 1963 · 652 citations