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. 2019 Apr 19;20(8):1929. doi: 10.3390/ijms20081929

Figure 1.

Figure 1

tRNA molecules and corresponding aminoacyl-tRNAs that have been used to expand the genetic code of live cells. Crystal structures of tRNA molecules (in white) are shown in complex with the corresponding aminoacyl-tRNAs (in the colors of the rainbow). The labels next to each structure indicate the origin of the orthogonal tRNA/tRNA synthetase pair and an organism into which this pair has been transplanted, which is followed by a brief description of tRNA identity or anti-identity elements that make a tRNA/tRNA synthetase pair orthogonal in an organism into which this pair has been transplanted. For example, the label “TyrRS-tRNATyr—From S. cerevisiae to E. coli: G1-C72 in bacteria vs C1-G72 in eukaryotes” means that the TyrRS-tRNATyr pair has been transplanted from S. cerevisiae into E. coli where this pair remains orthogonal due to different identity elements between bacterial and eukaryotic tRNATyr: the G1-C72 pair in bacterial tRNATyr and the C1-G72 pair in eukaryotic tRNATyr. The asterisk next to the LysRS-tRNALys complex indicates that this model was produced by docking the crystal structure of tRNALys into the tRNA-binding pocket of LysRS. The most comprehensive list of orthogonal tRNA/tRNA synthetase pairs and their classes can be found in the Supplemental files of Ref. [1].