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. 2013 Jun 4;288(28):20702–20712. doi: 10.1074/jbc.M113.472837

FIGURE 1.

FIGURE 1.

Overall structure of apo mlLRH-1. A, graphic representation of mlLRH-1 LBD with α-helixes in orange, β-strands in yellow, and the six-residue rodent-derived amino acid replacement in red. The empty LBP cavity is depicted as a white transparent surface. Disordered residues are represented by a black dashed line. B, ESI-MS of mlLRH-1. Phospholipid peaks are labeled as PG with the acyl carbon tail lengths and unsaturation characterized by collision-induced dissociation. The y-axis is scaled relative to the most abundant peak observed in the spectra. C, FoFc electron density (red) contoured at −3σ for phosphatidylethanolamine modeled into the LBP of mlLRH-1. D, 2FoFc electron density contoured at 1σ showing the partially active confirmation of mlLRH-1 evidenced by the discontinuous electron density between helices 11 and 12.