Table 1

Data collection and refinement statistics

PZ:ZPI complex (PDB 3F1S)
Data collection  
    Space group P 21 21 21 
    Cell dimensions A = 68.56 Å, b = 96.51 Å, c = 117.08 Å, α = β = γ = 90° 
    Molecules in the asymmetric unit One PZ and one ZPI 
    Resolution, Å 44.63-2.3 (2.42-2.3) 
    I/σI 15.4 (1.5) 
    Total number of measured reflections 174 258 (10 388) 
    Total number of unique reflections 32 582 (3462) 
    Completeness, % 92.6 (69.4) 
    Multiplicity 5.3 (3.0) 
    R merge, % 6.7 (56.1) 
    R meas, % 8.0 (71.1) 
Refinement  
    R work 0.225 
    R free 0.270 
    No. of atoms  
        Protein 5143 
        Water 82 
        Citrate 13 
        Chloride 
Average B factor, Å2 29.2 
RMS deviation  
    Bond length, Å 0.0058 
    Bond angles, ° 0.936 
Ramachandran plot (residues)  
        Ramachandran favored, % 97.32 
        Ramachandran outliers 
MolProbity score 98th percentile* (n = 8909, 2.05-2.55 Å) 
PZ:ZPI complex (PDB 3F1S)
Data collection  
    Space group P 21 21 21 
    Cell dimensions A = 68.56 Å, b = 96.51 Å, c = 117.08 Å, α = β = γ = 90° 
    Molecules in the asymmetric unit One PZ and one ZPI 
    Resolution, Å 44.63-2.3 (2.42-2.3) 
    I/σI 15.4 (1.5) 
    Total number of measured reflections 174 258 (10 388) 
    Total number of unique reflections 32 582 (3462) 
    Completeness, % 92.6 (69.4) 
    Multiplicity 5.3 (3.0) 
    R merge, % 6.7 (56.1) 
    R meas, % 8.0 (71.1) 
Refinement  
    R work 0.225 
    R free 0.270 
    No. of atoms  
        Protein 5143 
        Water 82 
        Citrate 13 
        Chloride 
Average B factor, Å2 29.2 
RMS deviation  
    Bond length, Å 0.0058 
    Bond angles, ° 0.936 
Ramachandran plot (residues)  
        Ramachandran favored, % 97.32 
        Ramachandran outliers 
MolProbity score 98th percentile* (n = 8909, 2.05-2.55 Å) 

RMS indicates root mean square.

*

Among structures of comparable resolution, 100th percentile is the best, 0th percentile the worst.

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