Difference between revisions of "Part:BBa K1952001:Design"

 
 
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===Design Notes===
 
===Design Notes===
−
hydrazine synthase subunit 2
 
  
 +
This construct contains the coding sequence only, reverse translated from K. stuttgartiensis protein sequence, optimized for expression in E. coli, with subsequent removal of internal restriction sites and repetitive sequences.
  
  
 
===Source===
 
===Source===
  
−
hydrazine synthase subunit 2
+
K. stuttgartiensis protein sequence; GenBank CAJ73612.1 [https://www.ncbi.nlm.nih.gov/protein/91200563]
 +
 
 +
The DNA for this part was synthesized by Integrated DNA technologies
  
 
===References===
 
===References===
 +
 +
Kartal, B., et al (2011) Molecular Mechanism of Anaerobic Ammonium Oxidation. ''Nature'' Vol 479 [doi:10.1038/nature10453]

Latest revision as of 15:35, 29 October 2016


Hydrazine Synthase beta subunit


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1032
    Illegal BamHI site found at 501
    Illegal BamHI site found at 702
    Illegal BamHI site found at 825
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 178


Design Notes

This construct contains the coding sequence only, reverse translated from K. stuttgartiensis protein sequence, optimized for expression in E. coli, with subsequent removal of internal restriction sites and repetitive sequences.


Source

K. stuttgartiensis protein sequence; GenBank CAJ73612.1 [1]

The DNA for this part was synthesized by Integrated DNA technologies

References

Kartal, B., et al (2011) Molecular Mechanism of Anaerobic Ammonium Oxidation. Nature Vol 479 [doi:10.1038/nature10453]