Difference between revisions of "Part:BBa K1602036"
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+ | This part is capable to generate the protein Acetyl Esterase (<a href="https://parts.igem.org/Part:BBa_K1216002">BBa_K1216002</a>). To fuse the protein to an <i>in vitro</i> scaffold (<a href="https://parts.igem.org/Part:BBa_K1602027">BBa_K1602027</a>) a linker-ligand sequence was added. This fusion could optimize the enzymatic degradation of Xylose by bringing the respective enzymes in spatial proximity. The ligand of this part binds to the SH3 domain of the scaffold. The construct also contains a strong Ribosome Binding Site (<a href="https://parts.igem.org/Part:BBa_B0034">BBa_B0034</a>). | ||
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Revision as of 02:45, 19 September 2015
Inducible generator of aes-SH3lig
This part is capable to generate the protein Acetyl Esterase (BBa_K1216002). To fuse the protein to an in vitro scaffold (BBa_K1602027) a linker-ligand sequence was added. This fusion could optimize the enzymatic degradation of Xylose by bringing the respective enzymes in spatial proximity. The ligand of this part binds to the SH3 domain of the scaffold. The construct also contains a strong Ribosome Binding Site (BBa_B0034). |
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 56
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 980