Journal of Bacteriology · 2008 · 131 citations · 11 references
Life SciencesBiochemistryMolecular BiologyEnzymologyMicrobial GeneticsStructural BiologyEnzyme FunctionEnzyme-substrate RecognitionMutagenesis StrategiesProtein StructureProtein TargetingSite-directed MutagenesisEfflux Pump GenesEfflux Pump MutationsEscherichia ColiMutagenesis Of Binding SitesPoint Mutation AnalysisPoint Mutation EffectsSite-directed Mutagenesis Of Surface ResiduesSubstrate Specificity Of Efflux Pumps
The Escherichia coli multidrug efflux pump protein AcrB has recently been cocrystallized with various substrates, suggesting that there is a phenylalanine-rich binding site around F178 and F615. We found that F610A was the point mutation that had the most significant impact on substrate MICs, while other targeted mutations, including conversion of phenylalanines 136, 178, 615, 617, and 628 to alanine, had smaller and more variable effects.
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Olga Lomovskaya, Mark S. Warren, Angela Lee et al. · Antimicrobial Agents and Chemotherapy · 2001 · 889 citations · Full text
Structural Asymmetry of AcrB Trimer Suggests a Peristaltic Pump Mechanism
Markus A. Seeger, A. Schiefner, Thomas Eicher et al. · Science · 2006 · 585 citations
Drug Export Pathway of Multidrug Exporter AcrB Revealed by DARPin Inhibitors
Gaby Sennhauser, Patrick Amstutz, Christophe Briand et al. · PLoS Biology · 2006 · 326 citations · Full text