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. 2013 Oct 24;42(2):1095–1110. doi: 10.1093/nar/gkt945

Figure 2.

Figure 2.

Deamination and binding assays with A3A and a 9-nt ssRNA. (A) Deamination of the single cytosine in the ssRNA oligonucleotide, AUUUCAUUU (JL1181, Table 1), was monitored by following the 13C-5-1H resonances of cytosine and uracil in 2D 1H-13C HSQC spectra. The total reaction time is indicated at the top right. Binding isotherms for representative HN resonances (B) and mapping of the binding site onto the A3A structure (C) for ssRNA (AUUUCAUUU) interacting with A3A, monitored by 1H-15N HSQC spectroscopy. (D) Binding site of ssDNA ATTTCATTT mapped onto the A3A structure (16) for comparison. In (C) and (D), A3A residues whose resonances exhibit large 1H,15N-combined chemical shift changes on nucleotide addition are colored red (> 0.05 p.p.m.) and orange (0.028–0.050 p.p.m.).