Cg-OxyR disulfide formation reorganizes its tetrameric conformation.

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Cg-OxyR disulfide formation reorganizes its tetrameric conformation. Cg-OxyR disulfide formation reorganizes its tetrameric conformation. (A) Crystal structure of reduced tetrameric Cg-OxyRC206S and a close-up view of the S206 and C215 of a single protomer (Right). (B) Crystal structure of the disulfide tetrameric Cg-OxyRSS, generated by crystallographic symmetry, with a close-up of the disulfide-bonded C206-C215 of a single protomer (Right). For both structures, each protomer is colored separately, and the RD homodimer formed by the blue and light-blue protomers were aligned before figure preparation, thereby providing a common orientation for structural comparison. (C) Each panel is a focused view of the relative positions of S206/C206 and C215 of the three crystal structures reported in this study. A structural alignment of all three structures was performed to provide a common orientation. The Left panel depicts the S206 and C215 of Cg-OxyRC206S, and is equivalent to the fully folded state of Cg-OxyRH2O2. The Center panel shows the locally unfolded state of Cg-OxyRH2O2, and the Right panel shows the C206-C215 disulfide of Cg-OxyRSS. Brandán Pedre et al. PNAS doi:10.1073/pnas.1807954115 ©2018 by National Academy of Sciences