Difference between revisions of "Part:BBa K133015"

 
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<partinfo>BBa_K133015 short</partinfo>
 
<partinfo>BBa_K133015 short</partinfo>
  
CF215 is the C-terminal portion of chimeric fusion protein; it contains the  C-terminal segment of the hypervariable region of H. pylori flagellin FlaA from 215 AA + 99 AA of C-terminal portion from E. coli flagellin; useful for inserting protein segments into the chimeric flagellin (example: CF213-multiepitope-CF215). In combination with CF213 it forms a TLR5 activating protein.
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CF215 is the C-terminal portion of chimeric fusion protein; it contains the  C-terminal segment of the hypervariable region of <i>H. pylori</i> flagellin FlaA from 215 AA + 99 AA of C-terminal portion from <i>E. coli</i> flagellin; useful for inserting protein segments into the chimeric flagellin (example: CF213-multiepitope-CF215). In combination with CF213 it forms a TLR5 activating protein.
  
 
mCherry is a red fluorescent protein that can be used for localisation studies.
 
mCherry is a red fluorescent protein that can be used for localisation studies.
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Since the protein was designed to be produced, we additionally added RGD-Hisstop tag.
  
  

Latest revision as of 05:06, 30 October 2008

CF215-mCherry-RGD-Histop

CF215 is the C-terminal portion of chimeric fusion protein; it contains the C-terminal segment of the hypervariable region of H. pylori flagellin FlaA from 215 AA + 99 AA of C-terminal portion from E. coli flagellin; useful for inserting protein segments into the chimeric flagellin (example: CF213-multiepitope-CF215). In combination with CF213 it forms a TLR5 activating protein.

mCherry is a red fluorescent protein that can be used for localisation studies.

Since the protein was designed to be produced, we additionally added RGD-Hisstop tag.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 571
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 128
    Illegal BamHI site found at 639
    Illegal BamHI site found at 1603
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1638