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TitleTarget sites for the design of anti-trypanosomatid drugs based on the structure of dihydroorotate dehydrogenase.
Journal, issue, pagesCurr. Pharm. Des., Vol. 19, Page 2615-2627, Year 2013
Publish dateMar 29, 2012 (structure data deposition date)
AuthorsPinheiro, M.P. / Emery, F.S. / Nonato, M.C.
External linksPubMed:23116399
MethodsX-ray diffraction
Resolution1.56 - 1.6 Å
Structure data

PDB-4ef8:
Crystal structure of dihydroorotate dehydrogenase from Leishmania major in complex with Phenyl isothiocyanate
Method: X-RAY DIFFRACTION / Resolution: 1.56 Å

PDB-4ef9:
Crystal structure of dihydroorotate dehydrogenase from Leishmania major in complex with 4-Nitrophenyl isothiocyanate
Method: X-RAY DIFFRACTION / Resolution: 1.6 Å

Chemicals

ChemComp-FMN:
FLAVIN MONONUCLEOTIDE

ChemComp-0FI:
N-phenylthioformamide

ChemComp-SO4:
SULFATE ION

ChemComp-GOL:
GLYCEROL

ChemComp-HOH:
WATER

ChemComp-4NF:
N-(4-nitrophenyl)thioformamide

Source
  • leishmania major (eukaryote)
KeywordsOxidoreductase/Oxidoreductase inhibitor / Leishmania major / dihydroorotate dehydrogenase / Phenyl isothiocyanate / pyrd / Oxidoreductase / Oxidoreductase-Oxidoreductase inhibitor complex / 4-Nitrophenyl isothiocyanate

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