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. 2017 Sep 22;114(41):E8703–E8710. doi: 10.1073/pnas.1704661114

Table S1.

Data collection and refinement statistics for CL40 Fab/gHgL/gp42(47–81) crystals

Anisotropy correction
Before After
Beamlines for screening/data collection 12–2 SSRL (SLAC)/21-ID-D LS-CAT (APS)
Wavelength, Å (energy, eV) 0.9998 Å (12,401 eV) at 21-ID-D, LS-CAT
Space group P 21 21 21
Unit cell dimensions
a, b, c, Å 96.38, 133.13, 254.13
 α, β, γ, ° 90, 90, 90
Data collection, XDS
 Resolution, Å 48.19–3.10 (3.21–3.10) 48.19–3.10 (3.21–3.10)
 Total reflections 897,266 (89,916) 891,949 (84,726)
 Unique reflections 60,129 (5,907) 60,099 (3,550)
 Redundancy 14.9 (15.2) 14.8 (14.4)
 Completeness, % 100 (100) 90.7 (56.7)
I/sI 11.7 (1.8) 11.4 (1.8)
 Wilson B-factor 76 59
Rmerge 0.219 (1.837) 0.216 (1.821)
 CC 1/2 0.998 (0.748) 0.998 (0.689)
 CC* 1.000 (0.925) 0.999 (0.903)
 Ellipsoid truncation resolution limits NA a*=3.6 Å, b*=2.9 Å, c*=3.0 Å
Refinement statistics (PHENIX 1.11.1–2575)
 Resolution, Å 22.74–3.10 (3.21–3.10)
 Reflections used 54,391 (3,343)
 Reflections used for Rfree 2,707 (161)
Rwork/Rfree 0.247/0.299
Number of atoms
 Total 18,663
 Protein 18,663
 Ligand/ion 0
 Water 0
B-factors
 Protein 61
 Ligand/ion NA
 Water NA
Ramachandran statistics
 Total accepted, % 99.7
 Outliers, % 0.3
rmsd
 Bond lengths, Å 0.003
 Bond angles, ° 0.63
Molprobity clashscore 4.3

Data collected from a single crystal. Values in parentheses are for the last resolution shell. R = Σ||Fobs| − |Fcalc||/Σ|Fobs|, where Rwork is calculated from this general formula using all reflections included in the refinement of the crystal structure model, and Rfree is calculated from a 5% random sample of reflections not included at any stage in the refinement of the crystal structure model. —, unchanged; NA, not applicable; XDS, X-ray detector software.