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. Author manuscript; available in PMC: 2021 Jun 7.
Published in final edited form as: Mol Cell. 2020 Dec 28;81(3):599–613.e8. doi: 10.1016/j.molcel.2020.11.047

Table 1.

Cryo-EM data collection, refinement, and validation statistics

MDA5-TRIM65PSpry-dsRNA RIG-I-RIPLETPSpry-dsRNA

Data collection and processing

Magnification 105,000 105,000
Voltage (kV) 300 300
Electron exposure (e−/Å2) 76.5/72.8 50
Defocus range (μm) −1.5 to −2.5 −0.7 to −2.5
Pixel size (Å) 0.85 0.855
Initial particle images (no.) 1,230,328 7,072,843

Refinement Filament Monomer Filament Monomer

PDB ID 7JL2 7JL0 7JL3 7JL1
EMDB ID EMD-22370 EMD-22368 EMD-22371 EMD-22369
Final particle images (no.) 15,306 49,051 39,718 74,079
Map resolution (Å) 4.3 4.3 4.2 3.9
FSC threshold 0.143 0.143 0.143 0.143
Model resolution (Å) 4.4 4.2 4.3 3.9
FSC threshold 0.5 0.5 0.5 0.5
Map sharpening B factor (Å2) −120 −113 −120 −103

Helical symmetry imposed

Twist (°) 86.941 76.1005
Rise (Å) 46.843 46.2706

Model composition

Non-hydrogen atoms 22,122 7352 21219 7132
Protein residues 2,526 842 2457 827
RNA nucleotides 88 28 84 28
Ligands 12 4 12 4

Root-mean-square deviations (RMSDs) from ideal

Bond lengths (Å) 0.006 0.008 0.003 0.010
Bond angles (°) 0.809 0.914 0.733 0.891

Validation

Clashscore 18.40 13.08 11.22 13.12
Poor rotamers (%) 0.55 0.14 1.45 0.00

Ramachandran plot (%)

Favored 94.67 93.29 97.10 95.65
Allowed 5.33 6.71 2.90 4.35
Disallowed 0.00 0.00 0.00 0.00