Difference between revisions of "Part:BBa K3128010"
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<partinfo>BBa_K3128010 short</partinfo> | <partinfo>BBa_K3128010 short</partinfo> | ||
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| + | ===Usage and Biology=== | ||
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Designing fusion proteins is sometimes tricky because of potential misfolding and... To avoid these problems, linkers are often used. Flexible linkers to enable a certain degree of movements of the fusion protein different parts. They are constituted with a succession of Gly and Ser residues. This linker has the following formula: (Gly-Gly-Ser)n, where n = 54 here. | Designing fusion proteins is sometimes tricky because of potential misfolding and... To avoid these problems, linkers are often used. Flexible linkers to enable a certain degree of movements of the fusion protein different parts. They are constituted with a succession of Gly and Ser residues. This linker has the following formula: (Gly-Gly-Ser)n, where n = 54 here. | ||
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In the iGEM Grenoble 2019 project, these linkers are used in order to have certain flexibility of the adenylate subparts fused to the OmpX proteins. Thus allowing the utilization of a bacterial two-hybrid system in the external membrane of the bacteria. | In the iGEM Grenoble 2019 project, these linkers are used in order to have certain flexibility of the adenylate subparts fused to the OmpX proteins. Thus allowing the utilization of a bacterial two-hybrid system in the external membrane of the bacteria. | ||
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Revision as of 12:40, 18 September 2019
Flexible Glycine Glycine Serine (GGS) Linker (54 aa)
Usage and Biology
Designing fusion proteins is sometimes tricky because of potential misfolding and... To avoid these problems, linkers are often used. Flexible linkers to enable a certain degree of movements of the fusion protein different parts. They are constituted with a succession of Gly and Ser residues. This linker has the following formula: (Gly-Gly-Ser)n, where n = 54 here. Sequences can be repeated in order to obtain an appropriate length separation of functional domains and can also be shortened to maintain inter-domain reactions. In the iGEM Grenoble 2019 project, these linkers are used in order to have certain flexibility of the adenylate subparts fused to the OmpX proteins. Thus allowing the utilization of a bacterial two-hybrid system in the external membrane of the bacteria.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]