Table 1 Cryo-EM data collection, refinement and validation statistics

From: Mechanistic insights into lanthipeptide modification by a distinct subclass of LanKC enzyme that forms dimers

 

Fully recognized PneKC (EMD-37514) (PDB 8WGO)

Pre-binding PneKC (EMD-37337) (PDB 8W7A)

LP-bound PneKC (EMD-37339) (PDB 8W7J)

Data collection and processing

   

Magnification

105 k

105 k

Voltage (kV)

300

300

Electron exposure (e–/Å2)

65.2

50

Defocus range (μm)

−1.0 to −2.0

−1.0 to −2.0

Pixel size (Å)

0.858

0.858

Symmetry imposed

C1

C1

Initial particle images (no.)

1,301,086

1,272,986

Final particle images (no.)

133,078

179,941

143,154

Map resolution (Å)

3.70

3.77

3.98

FSC threshold

0.143

0.143

0.143

Refinement

   

Initial model used (PDB code)

AlphaFold2

8WGO

8WGO

Model resolution (Å)

4.0

4.2

4.3

FSC threshold

0.5

0.5

0.5

Map sharpening B factor (Å2)

−187

−158.5

−182.1

Model composition

   

Non-hydrogen atoms

14,375

13,017

13,481

Protein residues

1753

1586

1641

Nucleotide residues

0

0

0

Ligands

4

1

3

B factors (mean, Å2)

   

Protein

100.30

79.71

125.60

Nucleotide

n.a.

n.a.

n.a.

Ligand

125.39

107.78

124.46

R.m.s deviations

   

Bond lengths (Å)

0.003

0.007

0.017

Bond angles (°)

0.662

1.115

1.652

Validation

   

MolProbity score

1.94

1.89

1.93

Clashscore

7.19

5.54

6.24

Poor rotamers (%)

0.19

0.00

0.14

Ramachandran plot

   

Favored (%)

90.30

88.37

88.41

Allowed (%)

9.35

10.67

11.10

Disallowed (%)

0.34

0.976

0.50