Table 1 Data collection and refinement statistics (molecular replacement)

From: Single amino acid substitution in Hendra virus attachment glycoprotein induces cross-neutralizing antibodies against Nipah virus

 

Nipah Virus attachment (G) glycoprotein in complex with neutralizing antibody 14F8

Hendra Virus attachment (G) glycoprotein mutant S586N

Hendra Virus attachment (G) glycoprotein mutant S586N in complex with neutralizing antibody 14F8

Data collection

 Space group

P 41 21 2

P 1 21 1

C 2 2 21

 Cell dimensions

 a, b, c (Å)

125.96 125.96 317.26

110.84 257.01193.52

110.84 257.01193.52

 α, β, γ (°)

90.00 90.00 90.00

90.00 97.69 90.00

90.00 90.00 90.00

 Resolution (Å)

36.45–2.79

41.59–3.30

37.79–3.22

 Rsym or Rmerge

0.10

0.148

0.214

 II

1.75 (at 2.81 Å)

3.08 (at 3.32 Å)

1.53 (at 3.25 Å)

 Completeness (%)

98.9

98.5

98.9

 Redundancy

13.2 (10.4)

6.2 (5.7)

5.1 (4.6)

Refinement

 Resolution (Å)

36.23–2.80

41.59–3.3

37.06–3.22

 No. reflections

63450

19266

44342

 Rwork/Rfree

21.93/24.35

23.2/28.13

19.45/22.74

 No. atoms

13483

6453

13414

 Protein

13096

6354

13086

 Ligand/ion

0

84

0

 Water

117

236

328

 B-factors

62.49

101.44

67.55

 Protein

62.59

101.28

66.63

 Ligand/ion

 

118.01

 

R.m.s. deviations

   

 Bond lengths (Å)

0.004

0.003

0.004

 Bond angles (°)

0.83

0.70

0.78

Ramachandran favored (%)

93.81

93.92

96.84

Ramachandran allowed (%)

6.19

6.08

3.16

Ramachandran outliers (%)

0

0

0

  1. The data for each structure is collected and analyzed from a single crystal. Statistics for the highest-resolution shell are shown in parentheses