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. Author manuscript; available in PMC: 2018 Jul 24.
Published in final edited form as: Nature. 2018 Jan 24;555(7695):269–273. doi: 10.1038/nature25758

Extended Data Table 2. Data collection and refinement statistics.

Highest resolution shell is shown in parentheses.

Structure Human DRD2 (ΔN/ΔICL3T4L/ΔC)-Risperidone complex

 Data Collection APS, GMCA/CAT 23ID-B/D, 10 μm microfocus beam

 Crystals 20
 Resolution range 30.00 - 2.90 (2.99 - 2.90)
 Space group P212121
 Unit cell Dimensions a, b, c (Å) 50.98 72.52 151.31
 Unique reflections 12826 (889)
 Multiplicity 5.5 (2.5)
 Completeness (%) 97.3 (86.9)
 Mean 1/σ(l) 15.2 (1.0)
 Rmerge (%) 13.4 (73.8)
 CC1/2(%) 99.4 (53.5)

Refinement Statistics
 Reflections used in refinement 12826 (889)
 Reflections used for R-free 622 (40)
 R-work (%) 22.6 (37.4)
 R-free (%) 24.9 (34.1)

Number of Atoms
 DRD2 1948
 T4L 1176
 Risperidone 30
 Lipid and other 82

Overall B-factors2)
 Receptor 84.1
 T4L 97
 Risperidone 75.8
 Lipids, water, other 86.8

Model Statistics
 RMSD-bonds (Å) 0.004
 RMSD-angles (°) 0.56
 Ramachandran favored (%)# 97.36
 Ramachandran allowed (%)# 2.64
 Ramachandran outliers (%)# 000
 Rotamer outliers (%)# 0.67
 Clashscore* 399
*

Rmerge = Σhkl |I(hkl) − <I(hkl)>|/Σhkl(hkl), where <I(hkl)> is the mean of the symmetry equivalent reflections of I(hkl).

#

As defined in MolProbity.