The integration of large quantities of biological information into mathematical models of cell metabolism provides a way for quantitatively evaluating the effect of parameter changes on simultaneous, coupled, and, often, counteracting processes. From a practical point of view, the validity of the model's predictions would critically depend on its quality. Among others, one of the critical steps that may compromise this quality is to decide which are the boundaries of the model. That is, we must decide which metabolites are assumed to be constants, and which fluxes are considered to be the inputs and outputs of the system. In this article, we analyze the effect of the experimental uncertainty on these variables on the system's characterization. Using a previously defined model of glucose fermentation in Saccharomyces cerevisiae, we characterize the effect of the uncertainty on some key variables commonly considered to be constants in many models of glucose metabolism, i.e., the intracellular pH and the pool of nucleotides. Without considering if this variability corresponds to a possible true physiological phenomenon, the goal of this article is to illustrate how this uncertainty may result in an important variability in the systemic responses predicted by the model. To characterize this variability, we analyze the utility and limitations of computing the sensitivities of logarithmic-gains (control coefficients) to the boundary parameters. With the exception of some special cases, our analysis shows that these sensitivities are good indicators of the dependence of the model systemic behavior on the parameters of interest.
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Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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Site | Modification | Modifier | Source | Reference |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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