Literature DB >> 2690819

An artificial-intelligence technique for qualitatively deriving enzyme kinetic mechanisms from initial-velocity measurements and its application to hexokinase.

L Garfinkel1, D M Cohen, V W Soo, D Garfinkel, C A Kulikowski.   

Abstract

We have developed a computer method based on artificial-intelligence techniques for qualitatively analysing steady-state initial-velocity enzyme kinetic data. We have applied our system to experiments on hexokinase from a variety of sources: yeast, ascites and muscle. Our system accepts qualitative stylized descriptions of experimental data, infers constraints from the observed data behaviour and then compares the experimentally inferred constraints with corresponding theoretical model-based constraints. It is desirable to have large data sets which include the results of a variety of experiments. Human intervention is needed to interpret non-kinetic information, differences in conditions, etc. Different strategies were used by the several experimenters whose data was studied to formulate mechanisms for their enzyme preparations, including different methods (product inhibitors or alternate substrates), different experimental protocols (monitoring enzyme activity differently), or different experimental conditions (temperature, pH or ionic strength). The different ordered and rapid-equilibrium mechanisms proposed by these experimenters were generally consistent with their data. On comparing the constraints derived from the several experimental data sets, they are found to be in much less disagreement than the mechanisms published, and some of the disagreement can be ascribed to different experimental conditions (especially ionic strength).

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Year:  1989        PMID: 2690819      PMCID: PMC1133561          DOI: 10.1042/bj2640175

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  25 in total

1.  The kinetics of enzyme-catalyzed reactions with two or more substrates or products. I. Nomenclature and rate equations.

Authors:  W W CLELAND
Journal:  Biochim Biophys Acta       Date:  1963-01-08

2.  Kinetic studies of yeast hexokinase.

Authors:  H J FROMM; V ZEWE
Journal:  J Biol Chem       Date:  1962-10       Impact factor: 5.157

3.  Ascites tumor mitochondrial hexokinase II. Effect of binding on kinetic properties.

Authors:  D P Kosow; I A Rose
Journal:  J Biol Chem       Date:  1968-07-10       Impact factor: 5.157

4.  The kinetics of yeast hexokinase in the light of the induced fit involved in the binding of its sugar substrate.

Authors:  G DelaFuente; A Sols
Journal:  Eur J Biochem       Date:  1970-10

5.  Structure of a complex between yeast hexokinase A and glucose. II. Detailed comparisons of conformation and active site configuration with the native hexokinase B monomer and dimer.

Authors:  W S Bennett; T A Steitz
Journal:  J Mol Biol       Date:  1980-06-25       Impact factor: 5.469

6.  Kinetic evidence that the high-affinity glucose 6-phosphate site on hexokinase I is the active site.

Authors:  L P Solheim; H J Fromm
Journal:  Arch Biochem Biophys       Date:  1981-10-01       Impact factor: 4.013

7.  Multiple hexokinases of rat tissues. Purification and comparison of soluble forms.

Authors:  L Grossbard; R T Schimke
Journal:  J Biol Chem       Date:  1966-08-10       Impact factor: 5.157

8.  Heart muscle hexokinase: subcellular distribution and inhibition by glucose 6-phosphate.

Authors:  S E Mayer; A C Mayfield; J A Haas
Journal:  Mol Pharmacol       Date:  1966-09       Impact factor: 4.436

Review 9.  Magnesium in cardiac energy metabolism.

Authors:  L Garfinkel; R A Altschuld; D Garfinkel
Journal:  J Mol Cell Cardiol       Date:  1986-10       Impact factor: 5.000

10.  Allosteric inhibition of brain hexokinase by glucose 6-phosphate in the reverse reaction.

Authors:  T Ureta; P A Lazo; A Sols
Journal:  Arch Biochem Biophys       Date:  1985-06       Impact factor: 4.013

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