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. 2022 Jul 8;50(14):8290–8301. doi: 10.1093/nar/gkac589

Table 1.

Cryo-EM collection and processing statistics

Data collection and processing Nsp15/dsRNA dataset 1 (EMD-26073, PDB: 7TQV) Nsp15/dsRNA dataset 2 (EMD-25915 PDB: 7TJ2)
Microscope Talos Arctica Titan Krios
Detector Gatan K2 Summit Gatan K3 Bioquantum
Nominal magnification 45 000× 81 000×
Voltage (kV) 200 300
Electron exposure (e2) 54 60
Defocus range (μm) −0.8 to -1.8 −1.2 to 2.2
Pixel size (Å) 0.93 0.53
Symmetry imposed C1 C1
Number of Micrographs 2435 752
Initial particle images 1 201 304 254 136
Final particle images 398 516 97 592
Refinement Dataset 1 Combined Datasets
Resolution (Å)/FSC threshold 3.43/0.143 3.19/0.143
B-factor used for map sharpening (Å2) 162.7 171.3
Map to model CC
CC (mask) 0.69 0.76
CC (volume) 0.68 0.74
CC (peaks) 0.56 0.65
CC (box) 0.68 0.69
Model composition
Non-hydrogen atoms 17 793 17 084
Protein residues 2083 2007
Nucleic acid 66 62
Mean B factors (Å2)
Protein 85.95 58.77
Nucleic acid 277.22 150.81
R.m.s. deviations
Bond lengths (Å) 0.002 0.002
Bond angles (°) 0.383 0.370
Validation
Molprobity score 1.52 1.39
Clashscore 5.00 3.74
Poor rotamers (%) 0.82 1.64
Ramachandran plot
Favored (%) 96.18 97.69
Allowed (%) 3.82 2.31
Disallowed (%) 0.00 0.00