Difference between revisions of "Part:BBa K4361319"

 
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<partinfo>BBa_K4361319 short</partinfo>
 
<partinfo>BBa_K4361319 short</partinfo>
  
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TBD main
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A mutant of the BlcR protein, created through site-directed mutagenesis with primers R1 ([[Part:BBa_K4361200]]) and F1.3 L38V ([[Part:BBa_K4361203]]). For this mutant, the leucine in position 38 has been changed to valine by mutating the TTG codon to GTG.
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This mutant also contains the following nucleotide mutations outside of the targeted site:
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<ul>
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<li>G 9 > T, resulting in substitution Q3H</li>
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<li>G 148 > T, resulting in a possible stop codon in position 50</li>
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<li>G 156 > C, silent mutation</li>
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<li>CGCG 198-201 > ATAT, resulting in substitution A67Y</li>
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<li>A 364 > T, resulting in substitution T122S</li>
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</ul>
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Sequencing data only contained this part's sequence up until and including nucleotide 399. All nucleotides after are presumed to be identical to those found in the original codon optimized BlcR, [[Part:BBa_K4361100]].
  
 
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Revision as of 12:26, 3 October 2022


BlcR L38V

A mutant of the BlcR protein, created through site-directed mutagenesis with primers R1 (Part:BBa_K4361200) and F1.3 L38V (Part:BBa_K4361203). For this mutant, the leucine in position 38 has been changed to valine by mutating the TTG codon to GTG.

This mutant also contains the following nucleotide mutations outside of the targeted site:

  • G 9 > T, resulting in substitution Q3H
  • G 148 > T, resulting in a possible stop codon in position 50
  • G 156 > C, silent mutation
  • CGCG 198-201 > ATAT, resulting in substitution A67Y
  • A 364 > T, resulting in substitution T122S

Sequencing data only contained this part's sequence up until and including nucleotide 399. All nucleotides after are presumed to be identical to those found in the original codon optimized BlcR, Part:BBa_K4361100.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 694
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 78
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 589