Difference between revisions of "Part:BBa K3505006"
Line 14: | Line 14: | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | <p style="text-align: center;"> | ||
+ | [[Image:T--Thessaly--GB-AATG-GCTT.jpeg|900px|thumb|none|]] | ||
+ | |||
<!-- --> | <!-- --> |
Revision as of 09:37, 13 October 2020
Tyr1-AIDAc Tyrosinase fused to membrane protein AIDAc. GB compatible B3-B5
Tyrosinase catalyzes the conversion of L-Tyrosine to L-Dopa and L-Dopa quinone. These derivatives can be detected electochemically, producing peak currents.[1] AIDA is native E.coli outer membrane protein. AIDA's CDS constists of 3 parts: [2] 1) A Signal Peptide that is cleaved in order the rest of the protein to be transported to the outer membrane. 2) The AIDAc is the autotransporter with the transmembrane part. 3) The passeger of AIDA which is the part that is on the exterior side.
We placed as passenger the Tyr1 gene coding to Rhizobium etli tyrosinase Because is the smallest of all tyrosinases (34kDa) and lack cysteines[3] compared to the melA tyrosinase BBa_K193600 used in iGEM before.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal PstI site found at 1487
Illegal PstI site found at 2073
Illegal NotI site found at 1211 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal BglII site found at 471
Illegal BamHI site found at 454
Illegal BamHI site found at 2337 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1439
Illegal EcoRI site found at 2135
Illegal XbaI site found at 1043
Illegal PstI site found at 1487
Illegal PstI site found at 2073
Illegal AgeI site found at 533 - 1000COMPATIBLE WITH RFC[1000]