Difference between revisions of "Part:BBa K2255005:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | |||
+ | D3 and the signal sequence are both the best conserved part from the attachment protein. So with protein global alignment (Needleman-Wunsch alignment), from two or three sequence at one time, we were eventually able to determinate D3 from M13. | ||
+ | We used iDT to optimise this sequence for ''E.coli''. | ||
===Source=== | ===Source=== |
Revision as of 16:55, 26 September 2017
Domain 3 of p3 from M13 (Rfc25)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
D3 and the signal sequence are both the best conserved part from the attachment protein. So with protein global alignment (Needleman-Wunsch alignment), from two or three sequence at one time, we were eventually able to determinate D3 from M13.
We used iDT to optimise this sequence for E.coli.
Source
The initial sequence came from E.coli M13 filamentous phages. But we modified the sequence with iDT optimisation codon.