Table 1 Crystallographic data collection and refinement statistics.

From: The structure of a tetrameric septin complex reveals a hydrophobic element essential for NC-interface integrity

 

Shs1-Cdc12-Cdc3-Cdc10

Data collection

Space group

C 1 2 1

Cell dimensions

 

a, b, c (Å)

258.178, 69.373, 92.533

α, β, γ (°)

90, 109.68, 90

Resolution (Å)

121.55–3.24 (3.65–3.24)a

Rmerge

0.521 (1.395)

I / σI

3.2 (1.5)

Completeness (%)

63.2 (10.7)b

Redundancy

6.6 (6.9)

Refinement

Resolution (Å)

121.55–3.24 (3.65–3.24)

No. reflections

15692 (82)

Rwork/Rfree

0.282/0.290

No. atoms

9086

Protein

8974

Ligand/ion

112

Water

0

B-factors

 

Protein

48.88

Ligand/ion

42.35

R.m.s. deviations

 

Bond lengths (Å)

0.003

Bond angles (°)

0.519

  1. A single crystal was used for the structure. Values in parentheses are for the highest-resolution shell.
  2. aHigh-resolution reflexes were included according to published criteria48,49.
  3. bThe traditional spherical completeness is given. The ellipsoidal completeness from the anisotropic analysis by autoPROC Staraniso41 is 88.0 (36.4) with diffraction limits of 3.24 Å, 3.42 Å and 4.33 Å along the reciprocal axes (0.934 a* − 0.358 c*), b* and (0.954 a* + 0.299 c*), respectively.