3PM1
Structure of QacR E90Q bound to Ethidium
Summary for 3PM1
Entry DOI | 10.2210/pdb3pm1/pdb |
Related | 1JT6 1JTY 1JUP 1JUS 3BQZ 3BR0 3BR1 3BR2 3BR4 3BR5 3BR6 |
Descriptor | HTH-type transcriptional regulator qacR, SULFATE ION, ETHIDIUM, ... (4 entities in total) |
Functional Keywords | tetr family member, transcription regulation, multidrug resistance, dna, nucleoid, transcription |
Biological source | Staphylococcus aureus |
Total number of polymer chains | 2 |
Total formula weight | 46866.72 |
Authors | Schumacher, M.A. (deposition date: 2010-11-15, release date: 2011-07-13, Last modification date: 2024-04-03) |
Primary citation | Peters, K.M.,Brooks, B.E.,Schumacher, M.A.,Skurray, R.A.,Brennan, R.G.,Brown, M.H. A single acidic residue can guide binding site selection but does not govern QacR cationic-drug affinity. Plos One, 6:e15974-e15974, 2011 Cited by PubMed: 21264225DOI: 10.1371/journal.pone.0015974 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.8 Å) |
Structure validation
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