Table 2 Data collection, processing, model refinement and validation

From: Structure-guided discovery of Otopetrin 1 inhibitors reveals druggable binding sites at the intrasubunit interface

 

DrOTOP1_C2.2

DrOTOP1_C11

DrOTOP_C2.36

Data collection and processing

Magnification

105,000

29,000

190,000

Voltage (kV)

300

200

200

Electron exposure (e–/Å2)

49.90

50.37

~ 40–50

Defocus range (μm)

−0.7 to −1.5

−0.8 to −1.8

−0.8 to −1.8

Pixel size (Å)

0.833

1.150

0.725

Initial particle images (no.)

6,147,309

3,410,686

7,236,014

Symmetry imposed

C2

C2

C2

Final particle images (no.)

155,580

164,766

290,491

Map resolution (Å)

3.23

3.73

3.42

 FSC threshold

0.143

0.143

0.143

 Map sharpening B factor (Å2)

−150.6

−102.2

−104.9

Model

Composition

 Peptide chains

2

2

2

 Protein residues

782

708

734

 Ligands

14

8

12

R.m.s. deviations

 Bond lengths (Å)

0.006

0.006

0.007

 Bond angles (°)

0.971

1.007

1.011

Validation

 MolProbity score

0.56

0.76

0.85

 Clashscore

0.15

0.85

1.30

 EMRinger score

2.39

1.9

2.13

 Poor rotamers (%)

0.00

0.65

0.00

Ramachandran plot

 Favored (%)

99.73

98.52

99.42

 Allowed (%)

0.27

1.48

0.58

 Disallowed (%)

0.00

0.00

0.00

Deposition ID

 EMDB

EMD-48227

EMD-48234

EMD-48235

 PDB

9MFF

9MFL

9MFM