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-Structure paper
Title | A single acidic residue can guide binding site selection but does not govern QacR cationic-drug affinity. |
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Journal, issue, pages | Plos One, Vol. 6, Page e15974-e15974, Year 2011 |
Publish date | Nov 15, 2010 (structure data deposition date) |
![]() | Peters, K.M. / Brooks, B.E. / Schumacher, M.A. / Skurray, R.A. / Brennan, R.G. / Brown, M.H. |
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Methods | X-ray diffraction |
Resolution | 2.8 Å |
Structure data | ![]() PDB-3pm1: |
Chemicals | ![]() ChemComp-SO4: ![]() ChemComp-ET: ![]() ChemComp-HOH: |
Source |
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![]() | TRANSCRIPTION / TetR family member / transcription regulation / multidrug resistance / DNA / nucleoid |