Multiplexed transcriptional repression identifies a network of bactericidal interactions between mycobacterial respiratory complexes
Open Access
- 4 December 2021
- Vol. 25 (1) , 103573
Abstract
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Funding Information
- Marsden Fund (UOO1807)
- Maurice Wilkins Centre for Molecular Biodiscovery
- Health Research Council of New Zealand (20/459)
- Royal Society Te Apārangi
This publication has 44 references indexed in Scilit:
- Inactivation of Fructose-1,6-Bisphosphate Aldolase Prevents Optimal Co-catabolism of Glycolytic and Gluconeogenic Carbon Substrates in Mycobacterium tuberculosisPLOS Pathogens, 2014
- Methylcitrate cycle defines the bactericidal essentiality of isocitrate lyase for survival of Mycobacterium tuberculosis on fatty acidsProceedings of the National Academy of Sciences, 2014
- Delayed bactericidal response of Mycobacterium tuberculosis to bedaquiline involves remodelling of bacterial metabolismNature Communications, 2014
- Discovery of Q203, a potent clinical candidate for the treatment of tuberculosisNature Medicine, 2013
- Regulation of proline metabolism in mycobacteria and its role in carbon metabolism under hypoxiaMolecular Microbiology, 2012
- Reduction of Clofazimine by Mycobacterial Type 2 NADH:Quinone OxidoreductaseJournal of Biological Chemistry, 2011
- Metabolomics of Mycobacterium tuberculosis Reveals Compartmentalized Co-Catabolism of Carbon SubstratesChemistry & Biology, 2010
- A Diarylquinoline Drug Active on the ATP Synthase of Mycobacterium tuberculosisScience, 2005
- Characterization of the cydAB -Encoded Cytochrome bd Oxidase from Mycobacterium smegmatisJournal of Bacteriology, 2001
- Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT MethodMethods, 2001