Skip to main content
. Author manuscript; available in PMC: 2021 Apr 27.
Published in final edited form as: Nat Struct Mol Biol. 2020 Jul 13;27(8):743–751. doi: 10.1038/s41594-020-0457-x

Table 2. Cryo-EM data collection, refinement and validation statistics of condensin +ATP states.

+ATP head segment (EMDB-10944) (PDB 6YVD) +ATP rod-shaped arm segment (EMD-10964)
Data collection and processing
Magnification 81,000 81,000
Voltage (kV) 300 300
Electron exposure (e–/Å2) 45 45
Defocus range (μm) –1.5 ~ –2.5 –1.5 ~ –2.5
Pixel size (Å) 1.70 1.70
Symmetry imposed C1 C1
Initial particle images (no.) 425,957 425,957
Final particle images (no.) 87,774 90,728
Map resolution (Å) FSC threshold 7.6 at 0.143 FSC threshold 8.2 at 0.143 FSC threshold
Map resolution range (Å) 6.5 – 10.5 7.5 – 11
Refinement
Initial model used (PDB code) Homology model derived from
5OQQ, 6QJ1, 6QJ2
Model resolution (Å) 8.4
   FSC threshold 0.143
Model resolution range (Å) n/a
Map sharpening B factor (Å2) -600
Model composition
   Non-hydrogen atoms 8,732
   Protein residues 1,760
   Ligands n/a
B factors (Å2)
   Protein 41.20
   Ligand n/a
R.m.s. deviations
   Bond lengths (Å) 0.007
   Bond angles (°) 1.410
Validation
   MolProbity score 1.30
   Clashscore 0.80
   Poor rotamers (%) 0.00
Ramachandran plot
   Favored (%) 89.94
   Allowed (%) 8.38
   Disallowed (%) 1.68