Difference between revisions of "Part:BBa K2319002:Design"
Raj Magesh (Talk | contribs) (→Design Notes) |
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===Source=== | ===Source=== | ||
− | + | <p>This short sequence was added using PCR, with primers having 5'-overhangs corresponding to these nucleotides.</p> | |
===References=== | ===References=== |
Latest revision as of 10:08, 1 November 2017
GGSGSGSS linker
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 10
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Serine, like threonine, has a hydroxyl group that contributes to stability by interacting with the aqueous cellular environment. Glycine, again due to its small size, maintains flexibility of the linker.
This linker region also contains a BamHI restriction site (G\GATCC) whose in-frame translation is Gly-Ser. This BamHI site is used to link our two protein domains during assembly of the fusion construct.
Source
This short sequence was added using PCR, with primers having 5'-overhangs corresponding to these nucleotides.