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Structure paper

TitleTwo Interacting Binding Sites for Quinacrine Derivatives in the Active Site of Trypanothione Reductase: A Template for Drug Design
Journal, issue, pagesJ. Biol. Chem., Vol. 279, Page 29493-, Year 2004
Publish dateApr 4, 2002 (structure data deposition date)
AuthorsSaravanamuthu, A. / Vickers, T.J. / Bond, C.S. / Peterson, M.R. / Hunter, W.N. / Fairlamb, A.H.
External linksJ. Biol. Chem. / PubMed:15102853
MethodsX-ray diffraction
Resolution2.7 Å
Structure data

PDB-1gxf:
CRYSTAL STRUCTURE OF TRYPANOSOMA CRUZI TRYPANOTHIONE REDUCTASE IN COMPLEX WITH THE INHIBITOR QUINACRINE MUSTARD
Method: X-RAY DIFFRACTION / Resolution: 2.7 Å

Chemicals

ChemComp-FAD:
FLAVIN-ADENINE DINUCLEOTIDE / FAD*YM

ChemComp-MAE:
MALEIC ACID

ChemComp-QUM:
QUINACRINE MUSTARD

ChemComp-HOH:
WATER

Source
  • trypanosoma cruzi (eukaryote)
KeywordsOXIDOREDUCTASE / TRYPANOTHIONE REDUCTASE / FAD DEPENDENT / DISULPHIDE OXIDOREDUCTASE / QUINACRINE MUSTARD / INHIBITOR / REDOX-ACTIVE CENTER / FLAVOPROTEIN / FAD / NADP

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