Comprehensive Analysis of Parasite Biology: From Metabolism to Drug Discovery 2016
DOI: 10.1002/9783527694082.ch20
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Mathematical Modeling and Omic Data Integration to Understand Dynamic Adaptation of Apicomplexan Parasites and Identify Pharmaceutical Targets

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Cited by 2 publications
(2 citation statements)
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“…Many efforts are ongoing, aiming to couple pharmacokinetic and constraint-based models to study drug-microbe-diet interactions [ 114 ]. However, a limitation of GSMM approach is that GEMs are stoichiometric models, and cannot, in their current form at least, incorporate metabolite concentrations or enzyme kinetics (V max , K m , K cat ) [ 115 , 116 ]. Albeit more limited in scope, kinetic modeling [ 116 ] may help improve understanding of the dynamics of metabolic pathways in the human gut.…”
Section: Concluding Remarks and Future Perspectivesmentioning
confidence: 99%
“…Many efforts are ongoing, aiming to couple pharmacokinetic and constraint-based models to study drug-microbe-diet interactions [ 114 ]. However, a limitation of GSMM approach is that GEMs are stoichiometric models, and cannot, in their current form at least, incorporate metabolite concentrations or enzyme kinetics (V max , K m , K cat ) [ 115 , 116 ]. Albeit more limited in scope, kinetic modeling [ 116 ] may help improve understanding of the dynamics of metabolic pathways in the human gut.…”
Section: Concluding Remarks and Future Perspectivesmentioning
confidence: 99%
“…With the rapid advancement of cutting-edge technologies in PBMC research, there is a growing need for development of integrative methods and computational models to cope with the increasing amounts of data. These approaches when applied at the systems level could mechanistically relate entities like gene, proteins and metabolites that might unveil the disease markers and related processes at the systems level (Sen et al, 2016 ).…”
Section: Genome-scale Metabolic Models As a Tool To Study Metabolismmentioning
confidence: 99%