Coding

Part:BBa_K2910006:Design

Designed by: Dimitrije Ratkov   Group: iGEM19_Toronto   (2019-10-16)
Revision as of 07:24, 20 October 2019 by Ratkovdi (Talk | contribs)

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IsPETase-T88I-I208Y-S238F-N241T-S245Y-R280T with C-terminal Hexahistidine Tag


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 67
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Two computational tools were used to inform the rational design process: FlexddG, a Rosetta protein design algorithm which can take backbone flexibility into account, and which gives an accurate prediction of the energy change after mutation; and FuncLib, a web server which can quickly and exhaustively screen combinations of mutants.

FlexddG was used to test substitutions at each candidate position. These were selected on a rational basis, to better interact with local motifs on the PET ligand. The best performers were fed into FuncLib; the most commonly substituted amino acids in the top 600 sequences as scored by FuncLib were used to put together a short-list of multiple mutants, which were tested using FlexddG again. This sequence was a Top 4 performer in this final testing process.

A detailed description of this process is available on the iGEM Toronto 2019 Wiki.


Source

This part came from the PDB crystal structure 5XJH fed into the algorithm above, followed by back-translation into DNA sequence using EMBOSS-Backtranseq.

References