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. Author manuscript; available in PMC: 2015 Dec 24.
Published in final edited form as: Angew Chem Int Ed Engl. 2005 May 30;44(22):3412–3415. doi: 10.1002/anie.200500075

Figure 1.

Figure 1

a) Secondary structure of TAR (transactivation response element) RNA in which the wild-type loop is replaced by a UUCG counterpart. The highlighted residues undergo Δδ>0.1 ppm changes in 1H NMR chemical shifts upon binding to neomycin B (yellow) and acetylpromazine (□). b,c) Structures and TAR-dissociation constants (Kd) for neomycin B (b; NeoB)[9, 11] and acetylpromazine (c; AcP).[14]