This thesis addresses antibacterial resistance by utilizing chemical proteomics in three projects. Project 1 optimizes new tuberculosis drugs, resulting in a more potent compound. Project 2 examines Chlorotonil, identifying its mode of action and a unique resistance mechanism. Project 3 explores nucleotide promiscuity of AMPylators, during infection. These projects showcase the power of chemical proteomics in unraveling complex bacterial pathways and discovering innovative antibacterial drug mechanisms.
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This thesis addresses antibacterial resistance by utilizing chemical proteomics in three projects. Project 1 optimizes new tuberculosis drugs, resulting in a more potent compound. Project 2 examines Chlorotonil, identifying its mode of action and a unique resistance mechanism. Project 3 explores nucleotide promiscuity of AMPylators, during infection. These projects showcase the power of chemical proteomics in unraveling complex bacterial pathways and discovering innovative antibacterial drug mec...
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