Table 1 PmScsC crystal structure statistics

From: Author Correction: A shape-shifting redox foldase contributes to Proteus mirabilis copper resistance

 

Compact (4XVW)

Transitional (5IDR)

Extended (5ID4)

Data collection

 Space group

P21

I4

H32

Cell dimensions

   a, b, c (Å)

137.5, 163.9, 181.9

193.1, 193.1, 105.8

86.7, 86.7, 330.9

   α, β, γ (º)

90, 90, 90

90, 90, 90

90, 90, 120

 Resolution (Å)

91.15–2.60 (2.74–2.60)

136.51–2.56 (2.57–2.56)

110.29–2.92 (2.93–2.92)

  Rmerge

0.072 (0.617)

0.083 (0.741)

0.059 (0.625)

  I /σI

11.0 (2.0)

14.9 (2.2)

14.2 (2.8)

  Completeness (%)

98.6 (95.4)

99.4 (100.0)

99.2 (100.0)

  Redundancy

3.8 (3.7)

4.1 (4.1)

4.1 (4.2)

Refinement

 Resolution (Å)

91.15–2.60

42.82–2.56

40.36–2.92

 No. of reflections

243,409

62,069

10,652

 Rwork/Rfree (%)

24.8/28.2

17.1/22.2

25.1/26.3

No. of atoms

   Protein

40,850

10,262

1720

   Ligand/ion

NA

NA

NA

   Water

281

82

0

B factors (Å2)

   Protein

59.7

50.6

122.2

   Ligand/ion

NA

NA

NA

   Water

41.5

43.0

NA

RMS deviations

   Bond length (Å)

0.006

0.008

0.010

   Bond angles (º)

1.21

1.05

1.17

  1. Single crystals were used to collect each dataset. Values for highest resolution shell are shown in parentheses