Efflux by Small Multidrug Resistance Proteins Is Inhibited by Membrane-interactive Helix-stapled Peptides

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Rationally Designed Transmembrane Peptide Mimics of the Multidrug Transporter Protein Cdr1 Act as Antagonists to Selectively Block Drug Efflux and Chemosensitize Azole-resistant Clinical Isolates ofCandida albicans

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Effect of hydrocarbon stapling on the properties of α-helical antimicrobial peptides isolated from the venom of hymenoptera

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Drug Efflux by a Small Multidrug Resistance Protein Is Inhibited by a Transmembrane Peptide

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New Substrates on the Block: Clinically Relevant Resistances for EmrE and Homologues

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Roles of Hydrophobicity and Charge Distribution of Cationic Antimicrobial Peptides in Peptide-Membrane Interactions

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Long-Acting Lipidated Analogue of Human Pancreatic Polypeptide Is Slowly Released into Circulation

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Control of Membrane Protein Topology by a Single C-Terminal Residue

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Inhibition of protein–protein interactions using designed molecules

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The Assembly Motif of a Bacterial Small Multidrug Resistance Protein

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Identification of a Glycine Motif Required for Packing in EmrE, a Multidrug Transporter fromEscherichia coli

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