Difference between revisions of "Part:BBa K3182001"
Line 28: | Line 28: | ||
[[Image:T--Linkoping Sweden--green2.jpeg|300px]] | [[Image:T--Linkoping Sweden--green2.jpeg|300px]] | ||
[[Image:T--Linkoping Sweden--fluorescnet.jpeg|300px]] | [[Image:T--Linkoping Sweden--fluorescnet.jpeg|300px]] | ||
+ | |||
+ | [[Image:T--Linkoping_Sweden--pinkplåster.jpeg|300px]] | ||
+ | [[Image:T--Linkoping_Sweden--CBD-sfGFPrör4.jpeg|300px]] | ||
+ | [[Image:T--Linkoping_Sweden--CBD-sfGFPbind.png|300px]] |
Revision as of 15:00, 21 July 2019
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 511
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Introduction
CBDcipA-GS+Thrombin linker
A cellulose binding domain (CBDcipA) from Clostridium thermocellum Cellulose scaffolding protein (CipA) which can be used to purify or attach proteins to cellulose, this part has a sfGFP fused to the CBDcipA. The part also has a flexible GS-linker (-GGGGSGGGGS-) with a thrombin site (-LVPRGS-, thrombin RS) added at the end, clevage with thrombin will add one glycine and one serine to the N-terminal of the C-terminal fusion protein of the CBDcipA.
Also added a BamHI recognition sequence (BamHI RS) to enable changeable fusion protein to the CBDcipA. BamHI was chosen because its RS codes for one glycine and one serine, fitting it to the end of the thrombin site, BamHI can also be used on dam/dcm methylated DNA, which is crucial to this part.
Mechanism of action