Difference between revisions of "Part:BBa K1456001"

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<partinfo>BBa_K1456001 short</partinfo>
 
<partinfo>BBa_K1456001 short</partinfo>
  
 
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<center>[[File:ATOMS-tpa results10.jpg|400px|]]</center><br/>
 
<ul>
 
<ul>
 
   <li>It has already been told that <b>this protein is the most potent and efficient thrombolytic agent popular in clinical practice.</b> It does this by activating plasminogen, a common anticoagulative factor zymogen found in normal bloodstream. By the conversion of plasminogen into plasmin, an enzyme that catalyzes the reaction of the cleavage of fibrin, the main clot component, <b>thrombolysis begins to degrade the clot.</b> (IUBMB Enzyme Nomeclature 1992; MetaCyc 2014) </li>
 
   <li>It has already been told that <b>this protein is the most potent and efficient thrombolytic agent popular in clinical practice.</b> It does this by activating plasminogen, a common anticoagulative factor zymogen found in normal bloodstream. By the conversion of plasminogen into plasmin, an enzyme that catalyzes the reaction of the cleavage of fibrin, the main clot component, <b>thrombolysis begins to degrade the clot.</b> (IUBMB Enzyme Nomeclature 1992; MetaCyc 2014) </li>

Revision as of 15:32, 21 October 2014

Human Tissue Plasminogen Activator (htPA)

ATOMS-tpa results10.jpg

  • It has already been told that this protein is the most potent and efficient thrombolytic agent popular in clinical practice. It does this by activating plasminogen, a common anticoagulative factor zymogen found in normal bloodstream. By the conversion of plasminogen into plasmin, an enzyme that catalyzes the reaction of the cleavage of fibrin, the main clot component, thrombolysis begins to degrade the clot. (IUBMB Enzyme Nomeclature 1992; MetaCyc 2014)
  • This activity has been shown synthetically in E.coli and experimentally in vitro. (Pennica et al. 1983; Van de Werf et al. 1984)


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 5
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 119
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 958