Difference between revisions of "Part:BBa K4593002:Design"
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===References=== | ===References=== | ||
[1] Lee, Chanyoung, et al. “Development of Advanced Chimeric Endolysin to Control Multidrug-Resistant Staphylococcus Aureus through Domain Shuffling.” ACS Infectious Diseases, vol. 7, no. 8, 28 May 2021, pp. 2081–2092. | [1] Lee, Chanyoung, et al. “Development of Advanced Chimeric Endolysin to Control Multidrug-Resistant Staphylococcus Aureus through Domain Shuffling.” ACS Infectious Diseases, vol. 7, no. 8, 28 May 2021, pp. 2081–2092. | ||
− | https://doi.org/10.1021/acsinfecdis.0c00812 | + | https://doi.org/10.1021/acsinfecdis.0c00812 |
Latest revision as of 23:40, 8 October 2023
ClyC
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 681
Illegal AgeI site found at 550 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
The sequence is codon optimized for expression in E. coli.
Source
Hybrid endolysin with CBD of LysPALS1 and EAD of LysSA12.
References
[1] Lee, Chanyoung, et al. “Development of Advanced Chimeric Endolysin to Control Multidrug-Resistant Staphylococcus Aureus through Domain Shuffling.” ACS Infectious Diseases, vol. 7, no. 8, 28 May 2021, pp. 2081–2092. https://doi.org/10.1021/acsinfecdis.0c00812