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10.1007/s12079-017-0429-z

http://scihub22266oqcxt.onion/10.1007/s12079-017-0429-z
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C5842191!5842191!29170885
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suck abstract from ncbi

pmid29170885      J+Cell+Commun+Signal 2018 ; 12 (1): 319-31
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  • The structure of the S-layer of Clostridium difficile #MMPMID29170885
  • Bradshaw WJ; Roberts AK; Shone CC; Acharya KR
  • J Cell Commun Signal 2018[Mar]; 12 (1): 319-31 PMID29170885show ga
  • The nosocomially acquired pathogen Clostridium difficile is the primary causative agent of antibiotic associated diarrhoea and causes tens of thousands of deaths globally each year. C. difficile presents a paracrystalline protein array on the surface of the cell known as an S-layer. S-layers have been demonstrated to possess a wide range of important functions, which, combined with their inherent accessibility, makes them a promising drug target. The unusually complex S-layer of C. difficile is primarily comprised of the high- and low- molecular weight S-layer proteins, HMW SLP and LMW SLP, formed from the cleavage of the S-layer precursor protein, SlpA, but may also contain up to 28 SlpA paralogues. A model of how the S-layer functions as a whole is required if it is to be exploited in fighting the bacterium. Here, we provide a summary of what is known about the S-layer of C. difficile and each of the paralogues and, considering some of the domains present, suggest potential roles for them.
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