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The next day, cells were pre-treated with phenformin, SR13800, and scyllo-inositol in concentrations of 50 M, 10 M, and 2 M, and atpenin A5 in concentrations of 10 M, 2 M, and 0.4 M

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Multiple research advancements of the complex structure of MmpL3 and its inhibitors indicate that most MmpL3 inhibitors are in the central pocket within the TMD and exert their activity by disrupting hydrogen bonding interactions between two conserved Asp-Tyr pairs, resulting in blocking the proton motive force that drives substrate translocation

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