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. 2008 Oct 16;36(20):6548–6557. doi: 10.1093/nar/gkn703

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© 2008 The Author(s)

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 6. — Codon binding by -Ψ₂₇ and the -Ψ₂₇;f⁵C₃₄. The equilibrium binding of the two ASLs to the cognate and noncognate codons, AUG and AUA respectively, was assessed using programmed E. coli ribosomes. (The ASL unmodified and the wobble position is designated ‘Ψ₂₇’; ASL modified at the wobble position is designated as ‘Ψ₂₇;f⁵C₃₄’.) The ASLs were bound to the A-site with E. coli bound to its cognate codon in the P-site. The ASLs were bound to the P-site with the bound to its cognate codon in the A-site.

Inline graphic — Codon binding by -Ψ₂₇ and the -Ψ₂₇;f⁵C₃₄. The equilibrium binding of the two ASLs to the cognate and noncognate codons, AUG and AUA respectively, was assessed using programmed E. coli ribosomes. (The ASL unmodified and the wobble position is designated ‘Ψ₂₇’; ASL modified at the wobble position is designated as ‘Ψ₂₇;f⁵C₃₄’.) The ASLs were bound to the A-site with E. coli bound to its cognate codon in the P-site. The ASLs were bound to the P-site with the bound to its cognate codon in the A-site.