Targeting persistent tubercule bacilli has become an important challenge in the development of anti-tuberculous drugs. As the glyoxylate bypass is essential for persistent bacilli, interference with it holds the potential for designing new antibacterial drugs. We have developed kinetic models of the tricarboxylic acid cycle and glyoxylate bypass in Escherichia coli and Mycobacterium tuberculosis, and studied the effects of inhibition of various enzymes in the M. tuberculosis model.
- BIOMD0000000222.xml (SBML and XML document - 49 KB)
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This Model was originally imported from the EBI Biomodels: http://www.ebi.ac.uk/biomodels-main/BIOMD0000000222.
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Created: 29th Nov 2012 at 10:15
Last used: 14th Dec 2019 at 12:20