Extended Data Table 1 Statistics of diffraction data collection and refinement

From: De novo design of transmembrane fluorescence-activating proteins

  1. Each diffraction dataset was collected from a single crystal. Values in parentheses are for the highest resolution shell. Rmerge = ΣhΣi | Ih,i−Ih | /ΣhΣiIh,i, where Ih is the mean intensity of the i observations of symmetry related reflections of h. R = Σ|Fobs−Fcalc | /ΣFobs, where Fcalc is the calculated protein structure factor from the atomic model (Rfree was calculated with 5% of the reflections selected).
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