Skip to main content
. Author manuscript; available in PMC: 2025 Jun 24.
Published in final edited form as: Nature. 2024 Oct 30;635(8040):978–986. doi: 10.1038/s41586-024-08121-5

Extended Data Table 1 |.

CryoEM data collection, processing, and model refinement statistics

Data collection and processing

Magnification (nominal) 130,000

Voltage (kV) 300

Electron exposure (e−/Å2) 63

Defocus range (μm) 0.3-2.0

Pixel size (Å) 0.843

Processing type Global Local

Symmetry imposed C3 none

Initial particle images (no.) 381,075 497,199

Final particle images (no.) 165,733 209,164

Map resolution (Å) 2.6 3.2
  FSC threshold 0.143 0.143

Map sharpening B factor (Å2) 85.7 114.8

 

Refinement

Initial model used (PDB code) 7LXY 7SOB

Model resolution (Å) 2.8 3.4
  FSC threshold 0.5 0.5

Model composition
  Nonhydrogen atoms 26,337 4006
  Protein residues 3,768 496
  Glycan residues 60 9

B factors (Å2)
  Protein 34.9 17.0
  Glycans 22.7 21.9

R.m.s. deviations
  Bond lengths (Å) 0.01 0.01
  Bond angles (°) 1.03 1.03

 

Validation

MolProbity score 0.8 0.7

Clashscore 0.83 0.26

Rotamer outliers (%) 0.3 0.0

Privateer glycan issues (%) 0.0 0.0

Ramachandran plot
  Favored (%) 98.0 97.5
  Allowed (%) 2.0 2.5
  Outliers (%) 0.0 0.0

EMRinger score 4.9 5.1

 

Data Availability

EMDB EMD-45174 EMD-45175