Part:BBa_K2201208
cysteinyl-lysinyl-tRNA Synthetase/tRNA pair
This cysteinyl-lysinyl-tRNA Synthetase/tRNA pair is based on the work of Nguyen et al. (2011). It is originated from the pyrrolysyl-tRNA synthetase of Methanosarcina barkeri containing a C313V mutation.
Nε-L-cysteinyl-L-lysine (CL) is an amino acid containing a free 1,2-aminothiol group at its side chain. 1,2-aminothiols are an important part of the synthesis of D-Luciferin. D-Luciferin is the substrate of the luciferase of the firefly Photinus pyralis. The synthesis of D-Luciferin is based on a condensation reaction between CL and a cyanobenzothiazole derivative resulting in a covalent bond between two thiazole residues. We designed and synthesized the novel amino acid Nγ‑2‑cyanobenzothiazol‑6‑yl‑L‑asparagine which contains 6-amino-2-cyanobenzothiazole at its side chain. Additionally, we showed that both amino acids are able to undergo the mentioned condensation reaction enabling a system for highly specific binding between peptides and enzymes.
So this aminoacyl-tRNA Synthetase/tRNA pair an important part of our fusing tool.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 492
- 1000COMPATIBLE WITH RFC[1000]
None |