<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">2638</id>
  <title>T3D2597</title>
  <common-name>Toxin A (Clostridium difficile)</common-name>
  <description>Toxins A and B are toxins from Clostridium difficile; they are the major pathogenicity factors of the antibiotic-associated diarrhea and the pseudomembranous colitis. Toxins A and B belong to the large clostridial cytotoxins family. Toxins A and B are also classified in the A-B bacterial toxin family. They are single-chain protein toxins constituted with three domains: receptor-binding, translocation, and a catalytic domain exhibiting a glycosyltransferase activity. (A341 , A340)</description>
  <cas></cas>
  <pubchem-id></pubchem-id>
  <chemical-formula nil="true"/>
  <weight>308052.7650000041</weight>
  <appearance>Clear solution.</appearance>
  <melting-point></melting-point>
  <boiling-point></boiling-point>
  <density nil="true"/>
  <solubility>&gt;10 mg/mL</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure>Ingestion (L1816) ; inhalation (L1816) ; dermal (L1816)</route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity>Rho GTPases are activated by glucosylation (for example RhoA at Thr37). The toxins catalyze the transfer of a glucosyl moiety from UDP-glucose to the Rho GTPases. The covalent attachment of the glucose moiety to a conserved threonine within the effector region of the GTPases renders the Rho-GTPases functionally inactive. As a consequence, the actin cytoskeleton is disaggregated and this is accompanied by cell rounding and formation of an arborized morphology. (A341, A340)</mechanism-of-toxicity>
  <metabolism>Free toxin may be removed by opsonization via the reticuloendothelial system (primarily the liver and kidneys) or it may be degraded through cellular internalization via the lysosomes. Lysosomes are membrane-enclosed organelles that contain an array of digestive enzymes, including several proteases.</metabolism>
  <toxicity>LD50: 500 ng/kg (Intraperitoneal, Mouse) (A2855)</toxicity>
  <lethaldose></lethaldose>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>Toxins A and B are toxins from Clostridium difficile; they are the major pathogenicity factors of the antibiotic-associated diarrhea and the pseudomembranous colitis. (A341 , A340)</use-source>
  <min-risk-level></min-risk-level>
  <health-effects>Toxins A is an enterotoxin from Clostridium difficile and causes antibiotic-associated diarrhea and pseudomembranous colitis. (A341 , A340, L1730)</health-effects>
  <symptoms>Symptoms of Clostridium difficile infection include bloating, constipation, and diarrhea with abdominal pain, which may become severe. Latent symptoms often mimic some flu-like symptoms. (L1730)</symptoms>
  <treatment>The antibiotics metronidazole and vancomycin have been shown to be effective against Clostridium difficile. (L1730)</treatment>
  <created-at type="dateTime">2009-07-06T18:11:25Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:25:45Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia></wikipedia>
  <uniprot-id>P16154</uniprot-id>
  <kegg-compound-id></kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id></chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id></ctd-id>
  <stitch-id>Toxin A</stitch-id>
  <drugbank-id></drugbank-id>
  <pdb-id>2F6E</pdb-id>
  <actor-id></actor-id>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles nil="true"/>
  <moldb-formula nil="true"/>
  <moldb-inchi nil="true"/>
  <moldb-inchikey nil="true"/>
  <moldb-average-mass type="decimal" nil="true"/>
  <moldb-mono-mass type="decimal" nil="true"/>
  <origin>Exogenous</origin>
  <state>Liquid</state>
  <logp></logp>
  <hmdb-id></hmdb-id>
  <chembl-id></chembl-id>
  <chemspider-id></chemspider-id>
  <structure-image-file-name>2f6e_bio_r_500.jpg</structure-image-file-name>
  <structure-image-content-type>image/jpeg</structure-image-content-type>
  <structure-image-file-size type="integer">26351</structure-image-file-size>
  <structure-image-updated-at type="dateTime">2014-10-14T18:13:30Z</structure-image-updated-at>
  <biodb-id>BSEQ0008479</biodb-id>
  <synthesis-reference></synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
