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Crystallization and preliminary crystallographic studies of dihydrofolate reductase-thymidylate synthase from Trypanosoma cruzi, the Chagas disease pathogen

  • Penchit Chitnumsub
  • , Jirundon Yuvaniyama
  • , Thippayarat Chahomchuen
  • , Tirayut Vilaivan
  • , Yongyuth Yuthavong
  • National Science and Technology Development Agency (NSTDA)
  • Chulalongkorn University

Research output: Contribution to journal › Article › peer-review

12 Citations (Scopus)

Abstract

Trypanosoma cruzi dihydrofolate reductase-thymidylate synthase (TcDHFR-TS) was crystallized in complexes with the dihydrotriazine-based or quinazoline-based antifolates C-448, cycloguanil (CYC) and Q-8 in order to gain insight into the interactions of this DHFR enzyme with classical and novel inhibitors. The TcDHFR-TS-C-448-NDP-dUMP crystal belonged to space group C2221 with two molecules per asymmetric unit and diffracted to 2.37 Å resolution. The TcDHFR-TS-CYC, TcDHFR-TS-CYC-NDP and TcDHFR-TS-Q-8-NDP crystals belonged to space group P21 with four molecules per asymmetric unit and diffracted to 2.1, 2.6 and 2.8 Å resolution, respectively. Crystals belonging to the two different space groups were suitable for structure determination.

Original languageEnglish
Pages (from-to)1175-1178
Number of pages4
JournalActa Crystallographica Section F: Structural Biology and Crystallization Communications
Volume65
Issue number11
DOIs
Publication statusPublished - 2009

Keywords

  • Antifolates
  • Chagas disease
  • Dihydrofolate reductase-thymidylate synthase
  • Trypanosoma cruzi

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