Difference between revisions of "Part:BBa K1680022"

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<partinfo>BBa_K1680022 short</partinfo>
 
<partinfo>BBa_K1680022 short</partinfo>
  
This part contains the protein coding region for a fusion protein of Cre recombinase (BBa_K1680007) that is C- & N-terminal flanked with 145N Dronpa [[part:BBa_K1680006]] using a 9 amino acid Ser/Gly-linker [[part:BBa_K1680001]] and the scar (Ser/Thr) as spacer. The construct has an N-terminal NLS sequence [[part:BBa_K1680004]]. In the expressed construct the two Dronpa domains should form multimers leading to an inactivated Cre recombinase that is reversibly activatable by Dronpa illumination (see Zhou et al 2012).  
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This part contains the protein coding region for a fusion protein of Cre recombinase (BBa_K1680007) that is C- & N-terminal flanked with 145N Dronpa [[part:BBa_K1680006]] using a 9 amino acid Ser/Gly-linker [[part:BBa_K1680001]] and the scar (Ser/Thr) as spacer. The construct has an N-terminal NLS sequence [[part:BBa_K1680004]]. In the expressed construct the two Dronpa domains should form multimers leading to an inactivated Cre recombinase that is reversibly activatable by Dronpa illumination (see Zhou et al 2012).  
  
 
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Revision as of 01:35, 26 September 2015

Dronpa caged Cre with NLS


This part contains the protein coding region for a fusion protein of Cre recombinase (BBa_K1680007) that is C- & N-terminal flanked with 145N Dronpa part:BBa_K1680006 using a 9 amino acid Ser/Gly-linker part:BBa_K1680001 and the scar (Ser/Thr) as spacer. The construct has an N-terminal NLS sequence part:BBa_K1680004. In the expressed construct the two Dronpa domains should form multimers leading to an inactivated Cre recombinase that is reversibly activatable by Dronpa illumination (see Zhou et al 2012).

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 298
    Illegal BglII site found at 2050
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1163