Part:BBa_K2871000:Design
Map20, T3SS export signal peptide from Map gene
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 85
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The amino acid sequence of the signal is obtained from Charpentier & Oswald (2004) paper. The DNA sequence is synthesized by IDT. The short glycine-serine linker (GGSGSGSG) is added by PCR to decrease folding interaction with a target protein. As this part was designed to be an N-terminal fusion domain, the RFC25 suffix sequence is added to the standard RFC10 suffix, which allows in-frame fusion with other RFC25 protein parts. The registry will recognize it as incompatible with RFC25 because of AgeI site on the RFC25 suffix that we added intentionally. But in fact, we can use it directly as an RFC25 part.
Source
Synthetic sequence deduced from Amino acid Sequence from the Enteropathogenic E. coli strain E22. Described in the paper Charpentier & Oswald, 2004.
References
Charpentier & Oswald, 2004. Journal of Bacteriology. 'Identification of the Secretion and Translocation Domain of the Enteropathogenic and Enterohemorrhagic Escherichia coli Effector Cif, Using TEM-1 β-Lactamase as a New Fluorescence-Based Reporter' DOI: 10.1128/JB.186.16.5486-5495.2004 https://jb.asm.org/content/186/16/5486