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[Preprint]. 2023 Jun 20:2023.06.20.545796. [Version 1] doi: 10.1101/2023.06.20.545796

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Extended Data Fig. 4. — a) Schematic illustrating processing workflow to identify the location of flanking DNA for the double-bound SNF2h-nucleosome complex as described in Methods. The gold-standard FSC determined by cryoSPARC is plotted in blue (FSC threshold of 0.143 indicated with dotted line).

b) The double-bound SNF2h-nucleosome map surface colored by local resolution determined by cryoSPARC with FSC cutoff of 0.143.

c) Angular distribution plots for the double-bound SNF2h-nucleosome map.

d) Coulomb potential map of the double-bound SNF2h-nucleosome complex shown at different contour levels. As the contour level increases, the density for SNF2h at the SHL+2 position appears weaker than the density for SNF2h at the SHL-2 position.