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6GMU

Serum paraoxonase-1 by directed evolution with the L69G/H134R/F222S/T332S mutations

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID23-1
Synchrotron siteESRF
BeamlineID23-1
Temperature [K]100
Detector technologyCCD
Collection date2010-11-14
DetectorADSC QUANTUM 315
Wavelength(s)0.9724
Spacegroup nameP 43 21 2
Unit cell lengths94.318, 94.318, 142.410
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution33.308 - 2.700
R-factor0.1839
Rwork0.179
R-free0.22850
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3srg
RMSD bond length0.008
RMSD bond angle0.899
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX ((1.11.1_2575: ???))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.750
High resolution limit [Å]2.7002.700
Rmerge0.1570.853
Rmeas0.1630.886
Rpim0.0450.238
Number of reflections18335881
<I/σ(I)>16.532.96
Completeness [%]99.9100
Redundancy13.513.7
CC(1/2)0.927
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP2910.1M Bis-Tris Propane pH 6.5, 0.2M Sodium Bromide and 20% PEG 3350

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