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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Mycobacterium tuberculosis Dihydrofolate Reductase Reveals Two Conformational States and a Possible Low Affinity Mechanism to Antifolate Drugs

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Autor(es):
Bertacine Dias, Marcio Vinicius [1, 2] ; Tyrakis, Petros [1] ; Domingues, Romenia Ramos [2] ; Paes Leme, Adriana Franco [2] ; Blundell, Tom L. [1]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QA - England
[2] CNPEM, Lab Nacl Biociencias LNBio, BR-13083100 Sao Paulo - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Structure; v. 22, n. 1, p. 94-103, JAN 7 2014.
Citações Web of Science: 13
Resumo

Inhibition of the biosynthesis of tetrahydrofolate (THF) has long been a focus in the treatment of both cancer and infectious diseases. Dihydrofolate reductase (DHFR), which catalyzes the last step, is one of the most thoroughly explored targets of this pathway, but there are no DHFR inhibitors used for tuberculosis treatment. Here, we report a structural, site-directed mutagenesis and calorimetric analysis of Mycobacterium tuberculosis DHFR (MtDHFR) in complex with classical DHFR inhibitors. Our study provides insights into the weak inhibition of MtDHFR by trimethoprim and other antifolate drugs, such as pyrimethamine and cycloguanil. The construction of the mutant Y100F, together with calorimetric studies, gives insights into low affinity of MtDHFR for classical DHFR inhibitors. Finally, the structures of MtDHFR in complex with pyrimethamine and cycloguanil define important interactions in the active site and provide clues to the more effective design of antibiotics targeted against MtDHFR. (AU)

Processo FAPESP: 10/15971-3 - Caracterização estrutural de enzimas envolvidas em vias de biossíntese de antibióticos com interesse biotecnológico
Beneficiário:Marcio Vinicius Bertacine Dias
Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores