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Identification of New MmpL3 Inhibitors by Untargeted and Targeted Mutant Screens Defines MmpL3 Domains with Differential Resistance
Author(s) -
John T. Williams,
Elizabeth R. Haiderer,
Garry B. Coulson,
Kayla N. Conner,
Edmund L. Ellsworth,
Chao Chen,
Nadine Álvarez,
Wei Li,
Mary Jackson,
Thomas Dick,
Robert B. Abramovitch
Publication year - 2019
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.00547-19
Subject(s) - mutant , biology , mycolic acid , biochemistry , mycobacterium , genetics , gene , bacteria
TheMycobacterium tuberculosis mycolate flippase MmpL3 has been the proposed target for multiple inhibitors with diverse chemical scaffolds. This diversity in chemical scaffolds has made it difficult to predict compounds that inhibit MmpL3 without whole-genome sequencing of isolated resistant mutants.

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