Difference between revisions of "Part:BBa K3767001:Design"
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===Source=== | ===Source=== | ||
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===References=== | ===References=== |
Revision as of 15:45, 8 June 2021
Alkaline Phosphatase optimized for E. Coli w/ 40x catalytic activity
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We began our design from the BBa_K1216001 part registered by the iGEM13_ETH_Zurich team (2). From the translated sequence of this part, we realized there were two stop codons at the begin of the sequence which led us to question how reliable the sequence was. To test reliability, we ran a BLAST analysis of the BBa_K1216001 and ran a Seaview alignment on the top 50 most similar sequences in E. coli. Based on this alignment we noticed that BBa_K1216001 had a N-terminus overhang that was not similar to other sequences. This led us to research alkaline phosphatase expressed primarily in E. coli. From this research we found the sequence created by Le Du, et al (3) which we then aligned with BBa_K1216001 to compare similarities.