Additional file 4: Figure S4. of Quaternary structure of a G-protein-coupled receptor heterotetramer in complex with Gi and Gs (original) (raw)

2016

Abstract

Possible interfaces in A2AR homodimers in complex with Gs. In A–E, the A2AR homodimer was modeled through TM4 using the H1-receptor structure as template (A), through TM5 using the structure of squid rhodopsin (B), through TM4/5 using the β1-receptor structure (C), and via TM5/6 (D) and TM1 (E) using the μ-OR structure. TM helices 1, 4, and 5 involved in receptor dimerization are highlighted in dark blue, light blue, and gray, respectively. A2AR protomers bound to Gs (in gray) are shown in light green, whereas Gs-unbound A2AR protomers are shown in dark green. Rluc (blue) is attached to the N-terminal αN helix of Gs, and YFP (yellow) is attached to the C-terminal domain of the Gs-unbound A2AR protomer (light green). It is important to note that the position of YFP is highly dependent on the orientation of the long and highly flexible C-tail of A2AR (102 amino acids, Gln311–Ser412), which was modeled as described for the OXER [32] (see Additional file 9: Figure S9 for details). Despi...

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