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. Author manuscript; available in PMC: 2013 Oct 1.
Published in final edited form as: Nat Struct Mol Biol. 2013 Feb 24;20(4):447–453. doi: 10.1038/nsmb.2505

Table 1.

Data collection, phasing and refinement statistics

Native SeMet
Data collection
Space group P21212 P21212
Cell dimensions
a, b, c (Å) 123.2, 150.2, 53.9 123.2, 150.2, 53.9
α, β, γ (°) 90 90
Peak
Wavelength 0.97912 0.97912
Resolution (Å) 36.0-2.0 47.6-2.0
Rmerge (%) 3.1 (55) 5 (45)
II 66.0 (3.4) 55.2 (4.1)
Completeness (%) 100 100
Redundancy 9.4 (8.3) 6.6 (6.7)
Refinement
Resolution (Å) 36.0-2.0
No. reflections 68,728
Rwork/Rfree 18.4/22.4
No. atoms
 Protein 6,295
 Ligand/ion 24
 Water 812
B-factors
 Protein 30.0
 Ligand/ion 20.8
 Water 36.5
r.m.s deviations
 Bond lengths (Å) 0.007
 Bond angles (°) 1.045

One crystal was used for each data set. Values in parentheses are for highest-resolution shell.