Table 2 Data collection, molecular replacement, and structure refinement statistics

From: Molecular architecture of the PBP2–MreC core bacterial cell wall synthesis complex

Data set

PBP2

PBP2:MreC

Data collection

  X-ray source

BM30A

ID23EH2

  Detector

ADSC Q315R

MARCCD 225

  Wavelength (Å)

0.979526

0.87260

  Scan-range (o)

182

199

  Oscillation (o)

1

1

  Space group

P21

C2

  a (Å)

71.40

338.66

  b (Å)

140.96

48.34

  c (Å)

81.30

151.51

  β (°)

101.7

113.01

  Overall resolution (Å)

45.39–3.03

43.94–2.74

  No. observed/unique reflections

81345/27837

144817/52464

  High-resolution shell (Å)

3.21–3.03

2.90–2.74

  Completeness (%) (last shell)

90.8 (84.5)

86.5 (83.1)

  R sym (last shell)

12.0 (43.4)

7.3 (41.0)

  I/σ(I) (last shell)

12.15 (3.0)

19.84 (3.0)

  CC1/2

98.9 (85.4)

99.7 (89.9)

  Wilson plot B-factor (Å2)

37.46

45.79

Molecular replacement

 Mol/ASU

2(PBP2)

2(PBP2), 4(MreC)

 Balbes probability (%) (2(PBP2))

89.72

 Phaser LLG score (2(PBP2))

487

Refinement

 Initial R work/R free (%)

43.37/46.74

47.74/50.77

 Final R work/R free (%)

25.10/28.77

25.69/29.22

 RMS deviation, bond lengths (Å)

0.010

0.008

 RMS deviation, bond angles (°)

1.268

1.269

 Mean B-factor (Å2)

51.47

60.03

 No. of protein atoms

8332

13312

 No. of water molecules

24

69

 No. of sulfate molecules

3

 

 Residues in most favored/allowed region of Ramachandran plot (%)

99.8

99.8