Antibacterial potency of Type VI amidase effector toxins is dependent on substrate topology and cellular context

  1. Atanas Radkov
  2. Anne L Sapiro
  3. Sebastian Flores
  4. Corey Henderson
  5. Hayden Saunders
  6. Rachel Kim
  7. Steven Massa
  8. Samuel Thompson
  9. Chase Mateusiak
  10. Jacob Biboy
  11. Ziyi Zhao
  12. Lea M Starita
  13. William L Hatleberg
  14. Waldemar Vollmer
  15. Alistair B Russell
  16. Jean-Pierre Simorre
  17. Spencer Anthony-Cahill
  18. Peter Brzovic
  19. Beth Hayes
  20. Seemay Chou  Is a corresponding author
  1. University of California, San Francisco, United States
  2. University of Miami, United States
  3. InBios International, United States
  4. Pacific Northwest University of Health Sciences, United States
  5. Stanford University, United States
  6. Washington University in St. Louis, United States
  7. Newcastle University, United Kingdom
  8. University of Washington, United States
  9. Carnegie Mellon University, United States
  10. University of California, San Diego, United States
  11. Université Grenoble Alpes, France
  12. Western Washington University, United States
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  1. Atanas Radkov
  2. Anne L Sapiro
  3. Sebastian Flores
  4. Corey Henderson
  5. Hayden Saunders
  6. Rachel Kim
  7. Steven Massa
  8. Samuel Thompson
  9. Chase Mateusiak
  10. Jacob Biboy
  11. Ziyi Zhao
  12. Lea M Starita
  13. William L Hatleberg
  14. Waldemar Vollmer
  15. Alistair B Russell
  16. Jean-Pierre Simorre
  17. Spencer Anthony-Cahill
  18. Peter Brzovic
  19. Beth Hayes
  20. Seemay Chou
(2022)
Antibacterial potency of Type VI amidase effector toxins is dependent on substrate topology and cellular context
eLife 11:e79796.
https://doi.org/10.7554/eLife.79796