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. Author manuscript; available in PMC: 2011 May 5.
Published in final edited form as: Bioorg Med Chem. 2009 Aug 13;17(18):6496–6504. doi: 10.1016/j.bmc.2009.08.016

Figure 3.

Figure 3

Illustration of the differences in binding site residue composition of the hH1 and h5-HT2A receptors within the context of the β2AR-T4L crystal structure. Residues are truncated at the Cβ carbon atom (ball-and-stick representation) and are colored based on residue similarity as described in Fig. 2. For those positions whose residue identity differs, the H1 residue is listed first, followed by the 5-HT2A residue.