Difference between revisions of "Part:BBa K4623003"
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<partinfo>BBa_K4623003 short</partinfo> | <partinfo>BBa_K4623003 short</partinfo> | ||
− | TrwC is a type of relaxase, which participates in bacterial DNA binding and horizontal transfer of genomic material between bacteria​ [1]​. In vitro, it can specifically recognize the nic sequence (GGTGCGTATTGTCT^ATAGC) on ssDNA, causing it to break, and covalently bind to the ssDNA. | + | TrwC is a type of relaxase, which participates in bacterial DNA binding and horizontal transfer of genomic material between bacteria​ <sup>[1]</sup>​. In vitro, it can specifically recognize the nic sequence (GGTGCGTATTGTCT^ATAGC) on ssDNA, causing it to break, and covalently bind to the ssDNA. |
− | Therefore, TrwC relaxase possesses sequence specificity, orthogonality, and the ability to form a covalent bond with standard oligonucleotides. This provides a potential method in our project design that may be superior to existing protein-bound DNA nanostructures. The linkage of TrwC with ssDNA in vitro depends on | + | Therefore, TrwC relaxase possesses sequence specificity, orthogonality, and the ability to form a covalent bond with standard oligonucleotides. This provides a potential method in our project design that may be superior to existing protein-bound DNA nanostructures. The linkage of TrwC with ssDNA in vitro depends on Mg<sup>2+</sup>, so the reaction can be initiated by adding Mg<sup>2+</sup> in the mixed system. Conversely, adding EDTA can terminate the reaction and yield DNA-protein complexes <sup>[2]</sup>​. |
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Revision as of 12:33, 11 October 2023
TrwC, a protein linker to covalently link ssDNA 5' end
TrwC is a type of relaxase, which participates in bacterial DNA binding and horizontal transfer of genomic material between bacteria [1]. In vitro, it can specifically recognize the nic sequence (GGTGCGTATTGTCT^ATAGC) on ssDNA, causing it to break, and covalently bind to the ssDNA.
Therefore, TrwC relaxase possesses sequence specificity, orthogonality, and the ability to form a covalent bond with standard oligonucleotides. This provides a potential method in our project design that may be superior to existing protein-bound DNA nanostructures. The linkage of TrwC with ssDNA in vitro depends on Mg2+, so the reaction can be initiated by adding Mg2+ in the mixed system. Conversely, adding EDTA can terminate the reaction and yield DNA-protein complexes [2].
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 286
Illegal PstI site found at 604 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 286
Illegal PstI site found at 604 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 286
Illegal PstI site found at 604 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 286
Illegal PstI site found at 604 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 409
Illegal SapI.rc site found at 124