Difference between revisions of "Part:BBa K2549010:Design"
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===References=== | ===References=== | ||
+ | [1]Design of a Split Intein with Exceptional Protein Splicing Activity. | ||
+ | Stevens AJ, Brown ZZ, Shah NH, ..., Cowburn D, Muir TW. | ||
+ | J Am Chem Soc, 2016 Feb;138(7):2162-5 PMID: 26854538; DOI: 10.1021/jacs.5b13528 | ||
+ | [2]A promiscuous split intein with expanded protein engineering applications. | ||
+ | Stevens AJ, Sekar G, Shah NH, ..., Cowburn D, Muir TW. | ||
+ | Proc Natl Acad Sci U S A, 2017 Aug;114(32):8538-8543 PMID: 28739907; DOI: 10.1073/pnas.1701083114 |
Revision as of 12:54, 3 October 2018
split intein Cfa C
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 91
Illegal SapI.rc site found at 21
Design Notes
The 122-124 residues of Cfa is mutated from EKD to GEP.
Source
IDT(gBlock)
References
[1]Design of a Split Intein with Exceptional Protein Splicing Activity. Stevens AJ, Brown ZZ, Shah NH, ..., Cowburn D, Muir TW. J Am Chem Soc, 2016 Feb;138(7):2162-5 PMID: 26854538; DOI: 10.1021/jacs.5b13528 [2]A promiscuous split intein with expanded protein engineering applications. Stevens AJ, Sekar G, Shah NH, ..., Cowburn D, Muir TW. Proc Natl Acad Sci U S A, 2017 Aug;114(32):8538-8543 PMID: 28739907; DOI: 10.1073/pnas.1701083114