QacR−Cation Recognition Is Mediated by a Redundancy of Residues Capable of Charge Neutralization†

Lignende værker

• A Single Acidic Residue Can Guide Binding Site Selection but Does Not Govern QacR Cationic-Drug Affinity
  af: Peters, Kate M., et al.
  Udgivet: (2011)
• The Staphylococcal QacR Multidrug Regulator Binds a Correctly Spaced Operator as a Pair of Dimers
  af: Grkovic, Steve, et al.
  Udgivet: (2001)
• Structural basis for cooperative DNA binding by two dimers of the multidrug-binding protein QacR
  af: Schumacher, Maria A., et al.
  Udgivet: (2002)
• Transmembrane Helix 12 of the Staphylococcus aureus Multidrug Transporter QacA Lines the Bivalent Cationic Drug Binding Pocket
  af: Hassan, Karl A., et al.
  Udgivet: (2007)
• Analysis of Tryptophan Residues in the Staphylococcal Multidrug Transporter QacA Reveals Long-Distance Functional Associations of Residues on Opposite Sides of the Membrane
  af: Hassan, Karl A., et al.
  Udgivet: (2008)