<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">2637</id>
  <title>T3D2596</title>
  <common-name>Bifunctional hemolysin/adenylate cyclase (Bordetella pertussis)</common-name>
  <description>Pertussis adenylate cyclase toxin (ACT) is one of the numerous toxins from Bordetella pertussis, the agent of the whooping cough disease. Pertussis AC toxin belongs to the RTX bacterial toxin family. Pertussis AC toxin expresses haemolytic and calmodulin-dependent adenylate cyclase activities. (A344, A343, A342)</description>
  <cas>566070-83-5</cas>
  <pubchem-id></pubchem-id>
  <chemical-formula nil="true"/>
  <weight>177519.95500000162</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>After binding of the pertussis AC toxin to the cell, binding to calcium ions leads to the translocation of its adenylate cyclase domain into the cytoplasm, where, upon binding by calmodulin, it produces ultraphysiological levels of cAMP. (A344, A342)</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></toxicity>
  <lethaldose></lethaldose>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>Pertussis adenylate cyclase toxin (ACT) is one of the numerous toxins from Bordetella pertussis, the agent of the whooping cough disease. (A344, A343, A342)</use-source>
  <min-risk-level></min-risk-level>
  <health-effects>Pertussis adenylate cyclase toxin is an exotoxin produced by Bordetella pertussis, the agent of the whooping cough disease.(L1727)</health-effects>
  <symptoms>After an incubation period that is typically seven to ten days, pertussis in infants and young children is characterized initially by mild respiratory infection symptoms such as mild coughing, sneezing, and runny nose (catarrhal stage). After one to two weeks, the coughing develops into uncontrollable fits, each with five to ten forceful coughs, followed by a high-pitched "whoop" sound as the patient struggles to breathe in afterwards (paroxysmal stage). Coughing fits are commonly followed by vomiting, and can lead to malnutrition. Fits can occur on their own or can be triggered by eating; they usually occur in groups, with multiple episodes every hour around the clock. This stage lasts two to eight weeks, and sometimes longer. A gradual transition then occurs to the convalescent stage, which usually lasts one to two weeks. Common complications of the disease include pneumonia, encephalopathy, earache, and seizures. Infection in newborns is particularly severe, with a death risk of up to 3%, often caused by severe pulmonary hypertension. (L1728)</symptoms>
  <treatment>Treatment with an effective antibiotic (erythromycin or azithromycin) shortens the infectious period but does not generally alter the outcome of the disease; however, when treatment is initiated during the catarrhal stage, symptoms may be less severe. Three macrolides (erythromycin, azithromycin and clarithromycin) are used in the U.S. for treatment of pertussis; trimethoprim-sulfamethoxazole is generally used when a macrolide is ineffective or is contraindicated. (L1728)</treatment>
  <created-at type="dateTime">2009-07-06T18:11:24Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:25:45Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia></wikipedia>
  <uniprot-id>P0DKX7</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>Bifunctional hemolysin</stitch-id>
  <drugbank-id></drugbank-id>
  <pdb-id></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>1yrt_bio_r_500.jpg</structure-image-file-name>
  <structure-image-content-type>image/jpeg</structure-image-content-type>
  <structure-image-file-size type="integer">45465</structure-image-file-size>
  <structure-image-updated-at type="dateTime">2014-10-14T18:13:29Z</structure-image-updated-at>
  <biodb-id>BSEQ0009832</biodb-id>
  <synthesis-reference></synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
