Difference between revisions of "Part:BBa K1194004"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1194004 short</partinfo> | <partinfo>BBa_K1194004 short</partinfo> | ||
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<partinfo>BBa_K1194004 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1194004 SequenceAndFeatures</partinfo> | ||
+ | <DIV class='curation y2014'> | ||
+ | Registry curation: Circular specification | ||
+ | |||
+ | This part was defined with itself as the last subpart.<BR> | ||
+ | That subpart was deleted to make the specification legal. A better correction may be possible. | ||
+ | </div> | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Revision as of 18:30, 14 April 2014
pLuxR --> ompF --> Gb3 mimic
Gb3 mimic codes for a nine-amino acid peptide that has anti-Shiga toxin activity. It is coded downstream of ompF which is an periplasmic translocation signal peptide. The entire assembly is under control of an N-acyl homoserine lactone (AHL) dependent pLuxR promoter. The part, when translated, produces the Gb3 mimic peptide. The ompF signal peptide helps to transport Gb3 mimic into the extracellular space. Gb3 mimic neutralises the Shiga toxin by binding to it and sequestering it. Other teams can utilise the ompF signal peptide if they want to ensure extracellular secretion of their protein of interest, especially if it is a small peptide. The Gb3 mimic peptide, though specific for the Shiga toxin, can be used for toxicology studies in general. Particularly, it can be of use to create a peptide library to investigate anti-toxin activities of therapeutic peptides by molecular docking.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Registry curation: Circular specification
This part was defined with itself as the last subpart.
That subpart was deleted to make the specification legal. A better correction may be possible.