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Structural basis of ligand binding to UDP-galactopyranose mutase from Mycobacterium tuberculosis using substrate and tetrafluorinated substrate analogues.
J Am Chem Soc. 2015 Jan 28;137(3):1230-44. doi: 10.1021/ja511204p. Epub 2015 Jan 16.
J Am Chem Soc. 2015.
PMID: 25562380
Natural and Synthetic Flavonoids as Potent Mycobacterium tuberculosis UGM Inhibitors.
Villaume SA, Fu J, N'Go I, Liang H, Lou H, Kremer L, Pan W, Vincent SP.
Villaume SA, et al.
Chemistry. 2017 Aug 1;23(43):10423-10429. doi: 10.1002/chem.201701812. Epub 2017 Jul 11.
Chemistry. 2017.
PMID: 28497493
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Synthesis and evaluation of heterocycle structures as potential inhibitors of Mycobacterium tuberculosis UGM.
Maaliki C, Fu J, Villaume S, Viljoen A, Raynaud C, Hammoud S, Thibonnet J, Kremer L, Vincent SP, Thiery E.
Maaliki C, et al.
Bioorg Med Chem. 2020 Jul 1;28(13):115579. doi: 10.1016/j.bmc.2020.115579. Epub 2020 Jun 2.
Bioorg Med Chem. 2020.
PMID: 32546296
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The endogenous galactofuranosidase GlfH1 hydrolyzes mycobacterial arabinogalactan.
Shen L, Viljoen A, Villaume S, Joe M, Halloum I, Chêne L, Méry A, Fabre E, Takegawa K, Lowary TL, Vincent SP, Kremer L, Guérardel Y, Mariller C.
Shen L, et al.
J Biol Chem. 2020 Apr 10;295(15):5110-5123. doi: 10.1074/jbc.RA119.011817. Epub 2020 Feb 27.
J Biol Chem. 2020.
PMID: 32107309
Free PMC article.
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