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Using a Fragment-Based Approach to Identify Alternative Chemical Scaffolds Targeting Dihydrofolate Reductase from Mycobacterium tuberculosis.
ACS Infect Dis. 2020 Aug 14;6(8):2192-2201. doi: 10.1021/acsinfecdis.0c00263. Epub 2020 Jul 10.
ACS Infect Dis. 2020.
PMID: 32603583
Crystal structures of the closed form of Mycobacterium tuberculosis dihydrofolate reductase in complex with dihydrofolate and antifolates.
Ribeiro JA, Chavez-Pacheco SM, de Oliveira GS, Silva CDS, Giudice JHP, Libreros-Zúñiga GA, Dias MVB.
Ribeiro JA, et al. Among authors: libreros zuniga ga.
Acta Crystallogr D Struct Biol. 2019 Jul 1;75(Pt 7):682-693. doi: 10.1107/S205979831900901X. Epub 2019 Jul 4.
Acta Crystallogr D Struct Biol. 2019.
PMID: 31282477
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Folate biosynthesis pathway: mechanisms and insights into drug design for infectious diseases.
Bertacine Dias MV, Santos JC, Libreros-Zúñiga GA, Ribeiro JA, Chavez-Pacheco SM.
Bertacine Dias MV, et al. Among authors: libreros zuniga ga.
Future Med Chem. 2018 Apr 1;10(8):935-959. doi: 10.4155/fmc-2017-0168. Epub 2018 Apr 9.
Future Med Chem. 2018.
PMID: 29629843
Review.
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Structural Basis for the Interaction and Processing of β-Lactam Antibiotics by l,d-Transpeptidase 3 (LdtMt3) from Mycobacterium tuberculosis.
Libreros-Zúñiga GA, Dos Santos Silva C, Salgado Ferreira R, Dias MVB.
Libreros-Zúñiga GA, et al.
ACS Infect Dis. 2019 Feb 8;5(2):260-271. doi: 10.1021/acsinfecdis.8b00244. Epub 2018 Dec 28.
ACS Infect Dis. 2019.
PMID: 30556998
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