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  1. 1ut1 (4,833 bytes)
    11: ...diate adherence to the upper urinary tract. These adhesins bind to the Dr blood group antigen and also agglu...
    24: ...rinary tract and diarrheal infections. The Afa/Dr adhesins confer adherence to epithelial cells via interact...
  2. 1ut2 (4,706 bytes)
    11: ...diate adherence to the upper urinary tract. These adhesins bind to the Dr blood group antigen and also agglu...
    24: ...rinary tract and diarrheal infections. The Afa/Dr adhesins confer adherence to epithelial cells via interact...
  3. 2bs8 (3,934 bytes)
    16: Impact of natural variation in bacterial F17G adhesins on crystallization behaviour.,Buts L, Wellens A, ...
  4. 2bs7 (3,917 bytes)
    16: Impact of natural variation in bacterial F17G adhesins on crystallization behaviour.,Buts L, Wellens A, ...
  5. 2bsc (3,952 bytes)
    16: Impact of natural variation in bacterial F17G adhesins on crystallization behaviour.,Buts L, Wellens A, ...
  6. 2bsb (3,940 bytes)
    16: Impact of natural variation in bacterial F17G adhesins on crystallization behaviour.,Buts L, Wellens A, ...
  7. 1usq (4,908 bytes)
    11: ...diate adherence to the upper urinary tract. These adhesins bind to the Dr blood group antigen and also agglu...
    24: ...rinary tract and diarrheal infections. The Afa/Dr adhesins confer adherence to epithelial cells via interact...
  8. 1usz (4,823 bytes)
    11: ...diate adherence to the upper urinary tract. These adhesins bind to the Dr blood group antigen and also agglu...
    24: ...rinary tract and diarrheal infections. The Afa/Dr adhesins confer adherence to epithelial cells via interact...
  9. 1o9w (3,978 bytes)
    14: ...in domains of the F17-G, PapGII and FimH fimbrial adhesins all share the immunoglobulin-like fold of the str...
  10. 1o9v (4,032 bytes)
    14: ...in domains of the F17-G, PapGII and FimH fimbrial adhesins all share the immunoglobulin-like fold of the str...
  11. 2yo2 (4,443 bytes)
    13: ...ter membrane after export is complete. In complex adhesins, head and stalk domains may alternate several tim...
    15: ...er structures of complex trimeric autotransporter adhesins conserved in enterobacteria.,Hartmann MD, Grin I,...
  12. 2yo3 (4,612 bytes)
    14: ...ter membrane after export is complete. In complex adhesins, head and stalk domains may alternate several tim...
    16: ...er structures of complex trimeric autotransporter adhesins conserved in enterobacteria.,Hartmann MD, Grin I,...
  13. 1e07 (3,540 bytes)
    10: ...n intracellular signaling. Receptor for E.coli Dr adhesins.<ref>PMID:10864933</ref>
  14. 3zgi (4,636 bytes)
    14: ... components recognizing adhesive matrix molecules adhesins, despite very low sequence identity. An extended ...
  15. 1smd (5,378 bytes)
    24: ...ides potential sites for the binding of bacterial adhesins.
  16. 4b9j (3,540 bytes)
    13: ... type of fibre assembly is novel for CU assembled adhesins. We also show that both subunits in the fibre bin...
  17. 2yny (4,470 bytes)
    13: ...ter membrane after export is complete. In complex adhesins, head and stalk domains may alternate several tim...
    15: ...er structures of complex trimeric autotransporter adhesins conserved in enterobacteria.,Hartmann MD, Grin I,...
  18. 9cse (4,898 bytes)
    14: ...cterizing the ligand-binding domains of fibrillar adhesins is important for understanding how bacteria can c...
  19. 1jmm (4,210 bytes)
    24: Antigens I/II are large multifunctional adhesins from oral viridans streptococci that exert immuno...
  20. 1r19 (4,276 bytes)
    23: ...nd its environment. Some of these proteins act as adhesins and mediate bacterial attachment to host tissues....

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