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Structure paper

TitleStructural mechanisms of QacR induction and multidrug recognition.
Journal, issue, pagesScience, Vol. 294, Page 2158-2163, Year 2001
Publish dateAug 20, 2001 (structure data deposition date)
AuthorsSchumacher, M.A. / Miller, M.C. / Grkovic, S. / Brown, M.H. / Skurray, R.A. / Brennan, R.G.
External linksScience / PubMed:11739955
MethodsX-ray diffraction
Resolution2.54 - 2.98 Å
Structure data

PDB-1jt6:
Crystal structure of the multidrug binding protein QacR bound to dequalinium
Method: X-RAY DIFFRACTION / Resolution: 2.54 Å

PDB-1jtx:
Crystal structure of the multidrug binding transcriptional regulator QacR bound to crystal violet
Method: X-RAY DIFFRACTION / Resolution: 2.85 Å

PDB-1jty:
Crystal structure of the multidrug binding transcriptional regulator QacR bound to ethidium
Method: X-RAY DIFFRACTION / Resolution: 2.97 Å

PDB-1jum:
Crystal structure of the multidrug binding transcriptional repressor QacR bound to the natural drug berberine
Method: X-RAY DIFFRACTION / Resolution: 2.98 Å

PDB-1jup:
Crystal structure of the multidrug binding transcriptional repressor QacR bound to malachite green
Method: X-RAY DIFFRACTION / Resolution: 2.95 Å

PDB-1jus:
Crystal structure of the multidrug binding transcriptional repressor QacR bound to rhodamine 6G
Method: X-RAY DIFFRACTION / Resolution: 2.84 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-DEQ:
DEQUALINIUM

ChemComp-HOH:
WATER

ChemComp-CVI:
CRYSTAL VIOLET / antifungal, antibiotic*YM

ChemComp-ET:
ETHIDIUM

ChemComp-BER:
BERBERINE / alkaloid*YM

ChemComp-MGR:
MALACHITE GREEN / Antimicrobial*YM

ChemComp-RHQ:
RHODAMINE 6G

Source
  • staphylococcus aureus (bacteria)
KeywordsTRANSCRIPTION / mutlidrug binding recognition / QacR / Mulitdrug resistance / S. aureus / multidrug binding / repressor / QacA / multidrug recognition / multidrug recognition mechanism / cationic lipophilic drugs / berberine / plant alkaloid / natural drug / malachite green / multidrug binding protein / Rhodamine 6G

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