Figure 5.

Ensemble-averaged $R_{\mathrm{h}}$ values calculated from the SAXS-reweighted CALVADOS ensembles, compared with the $R_{\mathrm{h}}$ determined by PFG NMR diffusion (error bars represent the standard error from fitting the NMR data). We tested four approaches to calculate the $R_{\mathrm{h}}$ from atomic coordinates: the $R_{\mathrm{g}}$-dependent Nygaard equation ($R_{\mathrm{h}}^{\text{Nyg}}$, in blue), the Kirkwood-Riseman equation ($R_{\mathrm{h}}^{\text{KR}}$, in orange), HullRad ($R_{\mathrm{h}}^{\text{HR}}$, in green), and the Nygaard correction to the Kirkwood-Riseman equation ($R_{\mathrm{h}}^{\text{Nyg}-\text{KR}}$, in red). To see this figure in color, go online.