Difference between revisions of "Part:BBa K3610036"

 
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<partinfo>BBa_K3610036 short</partinfo>
 
<partinfo>BBa_K3610036 short</partinfo>
  
This part is the cell surface receptor BAK1 from A. thaliana fused with a GFP. The two protein coding sequences are fused together with a 15 amino acid linker, coding for glycin and serine.
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This part is the cell surface receptor BAK1 from A. thaliana fused with the N-terminal sequence of a split-mCherry protein. The two protein coding sequences are fused together with a 15 amino acid linker, coding for glycin and serine.
 
As a promoter a truncated version of the ADH1 version was used as it confers lower expression levels.
 
As a promoter a truncated version of the ADH1 version was used as it confers lower expression levels.
 
To mediate termination of transcription the ScENO2 terminator from S. cerevisiae was used.
 
To mediate termination of transcription the ScENO2 terminator from S. cerevisiae was used.
  
BAK1/GFP is designed for the expression of a the full length plant receptor BAK1 from A. thaliana together with a fluorescent GFP tag in yeast. This allows checking for the localization and the level of expression of the BAK1 protein in the yeast cell. Being the full length cell surface protein, the BAK1 sequence has its own signal sequence from the orignal organism.
 
  
 
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<!-- Add more about the biology of this part here

Revision as of 13:22, 5 October 2020


BAK1 ectodomain / mCherry N-terminal - for C. reinhardtii

This part is the cell surface receptor BAK1 from A. thaliana fused with the N-terminal sequence of a split-mCherry protein. The two protein coding sequences are fused together with a 15 amino acid linker, coding for glycin and serine. As a promoter a truncated version of the ADH1 version was used as it confers lower expression levels. To mediate termination of transcription the ScENO2 terminator from S. cerevisiae was used.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 93
    Illegal NheI site found at 925
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 855
  • 1000
    COMPATIBLE WITH RFC[1000]