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. 2020 May 6;9:e55853. doi: 10.7554/eLife.55853

Table 2. Cryo-EM data collection, refinement and validation statistics of CALHM6 and CALHM2.

Dataset 3
CALHM6_Ca2+
Dataset 4
CALHM2_Ca2+
10-mer 11-mer
Data collection and processing
Microscope FEI Tecnai G2 Polara FEI Tecnai G2 Polara
Camera Gatan K2 Summit + GIF Gatan K2 Summit + GIF
Magnification 37,313 37,313
Voltage (kV) 300 300
Electron exposure (e–/Å2) 40 55
Defocus range (μm) -0.8 to -3.0 -0.8 to -3.0
Pixel size (Å) 1.34 1.34
Initial particle images (no.) 216,859 417,612
Final particle images (no.) 98,104 63,310 N/A
Reconstruction strategy1* Std Std Std
Symmetry imposed C10 C11 C1
Global map resolution (Å)
FSC threshold 0.143
4.39 6.23 N/A
Map resolution range (Å) 4.3-5.1 5.0-7.0 N/A
Map sharpening B factor (Å2) -259 -435 N/A
EMDB identifier 10924 10925 N/A
Refinement N/A
Model resolution (Å)
FSC threshold 0.5
4.4 6.6
Model composition
Non-hydrogen atoms
Protein residues

19,560
2,520

21,516
2,772
B factors (Å2)
Protein

85

86
R.m.s. deviations
Bond lengths (Å)
Bond angles (°)

0.004
0.773

0.004
0.822
Validation
MolProbity score
Clash score
Poor rotamers (%)

2.14
16.18
0

2.15
17.75
0
Ramachandran plot
Favored (%)
Allowed (%)
Disallowed (%)

93.55
6.05
0.40

93.95
5.65
0.40
PDB identifier 6YTV 6YTX

*Std – standard reconstruction; Loc – localized reconstruction.