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. 2012 Nov 12;287(53):44667–44675. doi: 10.1074/jbc.M112.423202

TABLE 1.

Data collection, phasing, and refinement statistics

Data collection
    Protein name Psu-WT T123C-ΔCys-Psu
    Space group I422 I422
    Cell dimension
        a, b, c 148.75, 148.75, 63.37 149.61, 149.61, 62.7
        α, β, γ 90.0, 90.0, 90.0° 90.0, 90.0, 90.0°
    Resolution (Å)a 47.04–2.04 (2.11–2.04) 47.31–3.00 (3.78–3.00)
    Rmerge 0.057 (0.343) 0.116 (0.463)
    I/σ(I) 13.4 (3.7) 6.2 (2.0)
    Completeness (%) 98.5 (92.0) 95.5 (96.4)
    Redundancy 4.8 (4.6) 3.0 (3.0)

Refinement
    Protein name Psu-WT T123C-ΔCys-Psu
    Resolution (Å) 47.04–2.04 47.31–3.00
    Rcryst/Rfree 19.2/21.9 23.11/27.66
    No. of atoms 1705 1480
    Protein 1479 1480
    Ligand 10
    Water
    B-factor (Å2) 216
        Average 36.53 58.13
        Protein 35.79 58.13
        Ligand 31.42
        Water 40.52
    Root mean square deviations
        Bond length (Å) 0.007 0.011
        Bond angles 0.9° 1.2°
    Ramachandran statistics (%)
        Most favored 97.7 97.3
        Additionally allowed 2.3 2.7
        Disallowed 0 0

a Numbers in parentheses refer to the highest resolution shell with all data collected from a single crystal.