Figure 2 - full size

 

Figure 2.
Figure 2. Structural comparison of native aequorin, semi-synthetic aequorins, and calmodulin. (A) Superimposed structures of molecule A of native aequorin and semi-synthetic aequorins. Native, cp-, br-, i-, and n-aequorin are shown in yellow, pink, blue, sky blue, and green, respectively. Apoaequorins are shown as C trace models. Coelenterazine moieties are drawn as ball-and-stick models with same colors as above. The coelenterazine moiety and the loop region of EF-hands I, III, and IV are surrounded by red, light blue, green, and orange circles, respectively. W1 in native aequorin is drawn as a sphere model in cyan. The OH group of the 2-substituent of native coelenterazine is stabilized by a hydrogen-bonding network mediated by W1. W1 is absent in br-, i-, and n-aequorin. The cyclopentyl group at the C8 position of cp-coelenterazine can make neither a stacking interaction with Lys39 nor a - interaction with Trp108. This figure was prepared with MolScript (Kraulis 1991) and Raster3D (Merrit and Bacon 1997). (B) Superimposed structures of EF-hands I, III, and IV of aequorin. (1) The superimposed structures of EF-hands I (shown in sky blue circle in Fig. 2A: 20-37), III (shown in green circle in Fig. 2A: 113-130), and IV (shown in orange circle in Fig. 2A: 149-166). EF-hand IV in molecule A is colored cyan and EF-hand IV in molecule B is colored blue. EF-hands I and III are colored green and yellow-green, respectively. The blue dashed line, EF-IV(B2), is the loop structure of EF-hand-IV(B) superimposed onto the same region of EF-IV(A). (2) The superimposed structures of the EF-hand I loop (residues 20-37) of aequorin (green) and Ca^2+-bound (deep pink) and Ca^2+-unbound (cream) calmodulin. The Ca^2+ is drawn as a sphere. All figures were prepared with MolScript (Kraulis 1991). (C) Structure comparison between aequorin and calmodulin. The superimposed structures of aequorin (yellow-green) and Ca^2+-unbound calmodulin (cream). The traced region of aequorin is from Thr103 to Pro189. The traced region of calmodulin is from Ser81 to Lys148. The coelenterazine moiety (CZH) is drawn as a ball-and-stick model. Dashed lines appeared in the inside of the red circle are main-chain interactions, green dotted lines are interactions in aequorin, and cream ones are interactions in calmodulin.

The above figure is reprinted by permission from the Protein Society: Protein Sci (2005, 14, 409-416) copyright 2005.