Difference between revisions of "Part:BBa K3505023"
(→Usage and Biology) |
(→Usage and Biology) |
||
Line 7: | Line 7: | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
− | FFAR2 is a naturally found eukaryotic GPCR protein that exhibits high affinity for SCFAs (acetic, propionic and butyric acid). After background searching through the NCBI database, we have identified the gene coding sequences needed for the designing of this gene construct. More specifically, a vasopressin receptor 2 segment has been attached to the C-terminal of the receptor, as it mediates recruitment of a TEV tagged b-arrestin-2, along with a TEV cleavage site(TCS). | + | FFAR2 is a naturally found eukaryotic GPCR protein that exhibits high affinity for SCFAs (acetic, propionic and butyric acid)(Dogra, Sona, Kumar and Yadav, 2016). After background searching through the NCBI database, we have identified the gene coding sequences needed for the designing of this gene construct. More specifically, a vasopressin receptor 2 segment has been attached to the C-terminal of the receptor, as it mediates recruitment of a TEV tagged b-arrestin-2, along with a TEV cleavage site(TCS). |
===Design Notes=== | ===Design Notes=== |
Revision as of 19:25, 27 October 2020
FFAR2:V2tail:TCS GB compatible with B2-B3
Usage and Biology
FFAR2 is a naturally found eukaryotic GPCR protein that exhibits high affinity for SCFAs (acetic, propionic and butyric acid)(Dogra, Sona, Kumar and Yadav, 2016). After background searching through the NCBI database, we have identified the gene coding sequences needed for the designing of this gene construct. More specifically, a vasopressin receptor 2 segment has been attached to the C-terminal of the receptor, as it mediates recruitment of a TEV tagged b-arrestin-2, along with a TEV cleavage site(TCS).
Design Notes
The coding sequence was domesticated . We removed BsmBI ,BsaI , BtgZI, BpiI sites in order to be compatible with GoldenBraid and MoClo. The sequence is presents in pUPD2 and has overhangs compatible for Golden Braid cloning. The CDS has position B2-B5.
Verification of Cloning
Source
Synthesized by IDT.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 284
Illegal PstI site found at 864 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 284
Illegal PstI site found at 864 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 106
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 284
Illegal PstI site found at 864 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 284
Illegal PstI site found at 864
Illegal NgoMIV site found at 364 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 560
Illegal SapI site found at 815
Illegal SapI.rc site found at 17