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. 2017 Jul 4;8:15952. doi: 10.1038/ncomms15952

Table 1. Data collection and refinement statistics for Lnt.

  LntEco-Se* LntEco LntEcoC387A LntPae
PDB code 5N6H 5N6L 5N6M
         
Data collection
 Space group P212121 P212121 P212121 C2
 Cell dimensions        
  a, b, c (Å) 54.56, 142.44, 201.39 54.2, 142.3, 199.92 55.22, 142.95, 197.71 152.73, 39.23, 102.25
  α, β, γ (°) 90, 90, 90 90, 90, 90 90, 90, 90 90, 116.26, 90
 Beamline X10SA-PXII X10SA-PXII X10SA-PXII X06SA-PXI
 Wavelength (Å) 0.9792 1.0 1.0 1.0
 No. of crystals 3 3 3 2
 Total data (°) 450 540 160 300
 Resolution (Å) 50–3.97 (4.08–3.97) 50–2.90 (3.00–2.90) 50–2.90 (2.98–2.90) 50–3.10 (3.20–3.10)
Rmeas 0.29 (2.93) 0.34 (3.00) 0.24 (1.57) 0.28 (1.53)
II 8.97 (0.83) 9.52 (1.00) 7.72 (1.32) 6.50 (1.43)
 Completeness (%) 96.0 (66.2) 100 (100) 97.9 (86.3) 98.9 (99.2)
 Multiplicity 16.28 (10.91) 19.67 (20.40) 5.42 (3.55) 5.40 (5.51)
 CC1/2 0.99 (0.26) 0.99 (0.27) 0.99 (0.42) 0.98 (0.41)
 CCanom 0.3
 Mosaicity (°) 0.21 0.24 0.31 0.25
Phasing Se-SAD MR MR MR
 Resolution range (Å) 50–4.5      
 Heavy atoms sites 20 Se      
 Correlation coefficient (all/weak) 49.40/18.80      
         
Refinement
 Resolution (Å)   50–2.90 50–2.90 50–3.10
 No. of reflections Rwork/Rfree   35266/1763 34807/1699 10157/1005
Rwork/Rfree   0.22/0.25 0.23/0.26 0.22/0.27
 r.m.s. deviations        
  Bond lengths (Å)   0.003 0.004 0.004
  Bond angles (°)   0.728 0.798 0.855
 B-factor        
  Proteins chain A   72.38 78.49 64.97
  Proteins chain B   87.98 90.88
  Ligands        
   9.9 MAG   83.39 98.79 68.46
   Glycerol   93.07 99.31 73.66
   Citrate   86.67
  H2O   72.61 74.83 48.17
 Ramachandran Plot        
  Favoured (%)   96.48 97.68 95.26
  Allowed (%)   3.52 2.32 4.74
  Outliers (%)   0.00 0.00 0.00
 MolProbity Clash score   6.26 9.94 8.52

PDB, protein data bank.

*Data processing statistics is reported with Friedel pairs separated. Values in parentheses are for the highest resolution shell.