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. 2022 Nov 17;12(11):1705. doi: 10.3390/biom12111705

Figure 3.

Figure 3

Multiple sequence alignment of the structural group 9a toxins: AnmTX Sco 9a-1 (C0HM64) S. coccinea; Am-1 (P69929) from Antheopsis maculata [31]; hautx2 (A0A0P0UTI6) and hautx3 (A0A0P0UTQ7) from Heteractis aurora [32]; Pi-actitoxin-Ugr1a, U-actitoxin-Ugr1b, and U-actitoxin-Ugr1c (R4ZCU1) from Urticina grebelnyi [22]; U-actitoxin-Avd13a and U-actitoxin-Avd13b (P0DMZ8) from Anemonia viridis [33]; Bcg-III-23.41 (P86467) from Bunodosoma cangicum [34]; AnmTx-Ms-9a-1, AnmTx-Ms-9a-2 (A0A1R3S3A8), and AnmTx-Ms-9a-3 from Metridium senile [23]; SHTX-1/SHTX-2 (P0C7W7) from Stichodactyla haddoni [35]; and U-homostoxin-Hdu1a (C0HJB4) from Stichodactyla duerdeni [36]. Modified residue–hydroxyproline shown as O in sequences. Identical and conserved amino acid residues are shown on a dark and light gray background, respectively. Vector NTI Advance v. 11.0 (Invitrogen, Carlsbad, CA, USA) [37] was used for multiple sequence alignment.