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. Author manuscript; available in PMC: 2020 Oct 1.
Published in final edited form as: Neuropharmacology. 2019 Jun 28;157:107691. doi: 10.1016/j.neuropharm.2019.107691

Table 3. Alignment and nAChR selectivity profiles of native and mutated α-Ctxs homologous to VnIB.

Based on previously published data, up to four nAChRs subtypes, at which the given α-Ctxs has the highest potencies, are shown. The alignment was prepared using the ConoServer (Kaas et al., 2008). Conserved residues and residues conserved in >50% of sequences are shaded dark and light gray, respectively. α6 given in the table refers to the α6/α3 chimera. “≈” indicates a difference in IC50 < 2.5-fold. r, rat; h, human; m, mouse.

α-Ctx Alignment nAChR preference
VnIB G G C C S H P V C Y T KN P N-C G # rα6β4 > rα3β4 >> rα6β2β3a
OmIA - G C C S H P AC N V N N P H I C G # rα3β2 >/≈ rα7 > rα6β2β3b
AuIB - G C C S Y P P C F A T N P D- C - # rα3β4 > rα6β4 ≈ rα7c
PeIA[A7V,S9H,V10A,N11R] - G C C S H P V C H A R H P E L C - # rα6β2β3 > rα3β2, d
TxID - G C C S H P V C S A M S P I - C - # rα3β4 > rα6β4 >> rα2β4e
PeIA[A7V,S9H,V10A,N11R,E14A] - G C C S H P V C H A R H P A L C - # rα6β2β3 > rα6β4 >> rα3β2f
BnIA - G C C S H P A C S V N N P D I C - # hα7 > mα1β1γδ, g
RegIIA - G C C S H P A C N V N N P H I C - # rα3β2 > rα3β4 ≈ rα6β2* >/≈ rα7h