A Database of Thermodynamic Quantities for the Reactions of Glycolysis and the Tricarboxylic Acid Cycle
- 6 May 2010
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 114 (49) , 16068-16082
Abstract
Analysis of biochemical systems requires reliable and self-consistent databases of thermodynamic properties for biochemical reactions. Here a database of thermodynamic properties for the reactions of glycolysis and the tricarboxylic acid cycle is developed from measured equilibrium data. Species-level free energies of formation are estimated on the basis of comparing thermodynamic model predictions for reaction-level equilibrium constants to previously reported data obtained under different experimental conditions. Matching model predictions to the data involves applying state corrections for ionic strength, pH, and metal ion binding for each input experimental biochemical measurement. By archiving all of the raw data, documenting all model assumptions and calculations, and making the computer package and data available, this work provides a framework for extension and refinement by adding to the underlying raw experimental data in the database and/or refining the underlying model assumptions. Thus the resulting database is a refinement of preexisting databases of thermodynamics in terms of reliability, self-consistency, transparency, and extensibility.Keywords
This publication has 50 references indexed in Scilit:
- Experimentally observed phenomena on cardiac energetics in heart failure emerge from simulations of cardiac metabolismProceedings of the National Academy of Sciences, 2009
- BISEN: Biochemical Simulation EnvironmentBioinformatics, 2009
- Chapter 2 Multiple Ion Binding Equilibria, Reaction Kinetics, and Thermodynamics in Dynamic Models of Biochemical Pathways2009
- Detailed kinetics and regulation of mammalian NAD-linked isocitrate dehydrogenaseBiochimica et Biophysica Acta (BBA) - Proteins and Proteomics, 2008
- Thermodynamic properties of enzyme-catalyzed reactions involving cytosine, uracil, thymine, and their nucleosides and nucleotidesBiophysical Chemistry, 2007
- Thermodynamics-Based Metabolic Flux AnalysisBiophysical Journal, 2007
- Dynamics of Muscle Glycogenolysis Modeled with pH Time Course Computation and pH-Dependent Reaction Equilibria and Enzyme KineticsBiophysical Journal, 2006
- Putative regulatory sites unraveled by network‐embedded thermodynamic analysis of metabolome dataMolecular Systems Biology, 2006
- Biochemical thermodynamicsBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1994
- Thermodynamic Studies of the Formation and Ionization of the Magnesium(II) Complexes of ADP and ATP over the pH Range 5 to 91Journal of the American Chemical Society, 1966