Difference between revisions of "Part:BBa K2842669"
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<partinfo>BBa_K2842669 short</partinfo> | <partinfo>BBa_K2842669 short</partinfo> | ||
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− | + | This DNA construct encodes a C terminal segment of the AceL-TerL intein fused to the N terminus of a mScarlet reporter protein with a C terminal StrepTag for purification. The AceL-TerL intein acts as a protein ligase that forms a peptide bond between this protein and another protein bound to a complementary split intein, during this process the intein splices itself out of protein and is not present in the end fusion protein. This construct is a modular platform for the creation of split intein fusion proteins through the SapI restriction sites located immediately upstream and downstream of the mScarlet reporter. BBa_K2832680 was designed to be used in conjunction with this construct as it contains the corresponding N terminal intein segment to enable intein trans-splicing. | |
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Revision as of 16:49, 16 October 2018
mScarlet reporter with TerL-C intein on the N terminus
This DNA construct encodes a C terminal segment of the AceL-TerL intein fused to the N terminus of a mScarlet reporter protein with a C terminal StrepTag for purification. The AceL-TerL intein acts as a protein ligase that forms a peptide bond between this protein and another protein bound to a complementary split intein, during this process the intein splices itself out of protein and is not present in the end fusion protein. This construct is a modular platform for the creation of split intein fusion proteins through the SapI restriction sites located immediately upstream and downstream of the mScarlet reporter. BBa_K2832680 was designed to be used in conjunction with this construct as it contains the corresponding N terminal intein segment to enable intein trans-splicing.
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Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NotI site found at 941
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1224
Illegal BsaI.rc site found at 28
Illegal SapI site found at 1130
Illegal SapI.rc site found at 419