Difference between revisions of "Part:BBa K5102060:Design"
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+ | Cox, D. B. T. et al. RNA editing with CRISPR-Cas13. Science 358, 1019–1027 (2017). |
Latest revision as of 22:04, 30 September 2024
dPspCas13b fusion with ADAR2DD
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 235
Illegal PstI site found at 631
Illegal PstI site found at 1021
Illegal PstI site found at 2443
Illegal PstI site found at 3277
Illegal PstI site found at 3930 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 2884
Illegal PstI site found at 235
Illegal PstI site found at 631
Illegal PstI site found at 1021
Illegal PstI site found at 2443
Illegal PstI site found at 3277
Illegal PstI site found at 3930 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1787
Illegal BamHI site found at 839
Illegal BamHI site found at 3310
Illegal XhoI site found at 4011 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 235
Illegal PstI site found at 631
Illegal PstI site found at 1021
Illegal PstI site found at 2443
Illegal PstI site found at 3277
Illegal PstI site found at 3930 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 235
Illegal PstI site found at 631
Illegal PstI site found at 1021
Illegal PstI site found at 2443
Illegal PstI site found at 3277
Illegal PstI site found at 3930
Illegal AgeI site found at 1520
Illegal AgeI site found at 2396 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
The ADAR2DD sequence harbors two amino acid mutations: E488Q and T375G. While E488Q increases the adenosine-to- inosine editing rates, T375G confers increased specificity with slightly reduced activity.
Source
This part was ordered as a synthetic oligo from a DNA synthesis provider.
References
Cox, D. B. T. et al. RNA editing with CRISPR-Cas13. Science 358, 1019–1027 (2017).