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2012 disrupts FAK localization to focal adhesions After establishing lead peptide 2012 to be cell permeable and resistant to proteolytic cleavage, we began evaluating the ability of 2012 to act as a FAK FAT domain inhibitor and disrupt the cellular FAT-paxillin PPI

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The ESKAPE pathogens ( Enterococcus faecium , Staphylococcus aureus , Klebsiella pneumoniae , Acinetobacter baumannii , Pseudomonas aeruginosa and Enterobacter spp.) are particularly concerning because they can present simultaneous resistance against multiple classes of antibiotics 2