Table 1

Crystallographic data for the thrombin-protein C fragment complex

Buffer 0.1M Tris, pH 8.5, 0.2M CH3COONa 
PEG 4000 (30%) 
PDB ID 4DT7 
Data collection Raxis IV++ 
    Wavelength, Å 1.5418 
    Space group P21 
    Unit cell dimensions, Å a = 46.4, b = 84.3, c = 66.4 β = 94.6° 
    Molecules/asymmetric unit 
    Resolution range, Å 40-1.9 
    Observations 140 938 
    Unique observations 38 884 
    Completeness, % 97.8 (81.1) 
    Rsym, % 8.3 (34.0) 
    I/σ(I) 13.4 (2.4) 
Refinement  
    Resolution, Å 40-1.9 
    Rcryst, Rfree 0.175, 0.218 
    Reflections (working/test) 34 903/1953 
    Protein atoms 4755 
    Na+ 
    Solvent molecules 326 
    Rmsd bond lengths, Å 0.010 
    Rmsd angles, degrees 1.2 
    Rmsd ΔB (Å2), mm/ms/ssb 2.11/1.32/2.28 
    protein, Å2 30.0 
    Na+, Å2 26.3 
    solvent, Å2 36.9 
Ramachandran plot  
    Most favored, % 99.2 
    Generously allowed, % 0.2 
    Disallowed, % 0.6 
Buffer 0.1M Tris, pH 8.5, 0.2M CH3COONa 
PEG 4000 (30%) 
PDB ID 4DT7 
Data collection Raxis IV++ 
    Wavelength, Å 1.5418 
    Space group P21 
    Unit cell dimensions, Å a = 46.4, b = 84.3, c = 66.4 β = 94.6° 
    Molecules/asymmetric unit 
    Resolution range, Å 40-1.9 
    Observations 140 938 
    Unique observations 38 884 
    Completeness, % 97.8 (81.1) 
    Rsym, % 8.3 (34.0) 
    I/σ(I) 13.4 (2.4) 
Refinement  
    Resolution, Å 40-1.9 
    Rcryst, Rfree 0.175, 0.218 
    Reflections (working/test) 34 903/1953 
    Protein atoms 4755 
    Na+ 
    Solvent molecules 326 
    Rmsd bond lengths, Å 0.010 
    Rmsd angles, degrees 1.2 
    Rmsd ΔB (Å2), mm/ms/ssb 2.11/1.32/2.28 
    protein, Å2 30.0 
    Na+, Å2 26.3 
    solvent, Å2 36.9 
Ramachandran plot  
    Most favored, % 99.2 
    Generously allowed, % 0.2 
    Disallowed, % 0.6 

Rmsd indicates root-mean-squared deviation from ideal bond lengths and angles and Rmsd in B-factors of bonded atoms; mm, main chain-main chain; ms, main chain-side chain; and ss, side chain-side chain.

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