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5V0F

Crystal structure of C-As lyase with mutation K105A and substrate Roxarsone

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 5.0.2
Synchrotron siteALS
Beamline5.0.2
Temperature [K]100
Detector technologyCCD
Collection date2016-12-21
DetectorADSC QUANTUM 315
Wavelength(s)0.9999
Spacegroup nameP 43 21 2
Unit cell lengths41.730, 41.730, 119.140
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution39.384 - 2.230
R-factor0.1966
Rwork0.193
R-free0.26730
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5cb9
RMSD bond length0.016
RMSD bond angle1.735
Data reduction softwareiMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwarePHENIX (1.8.2_1309)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]41.7702.350
High resolution limit [Å]2.2302.230
Rmerge0.1280.863
Rmeas0.1450.960
Rpim0.0540.349
Number of reflections5438782
<I/σ(I)>9.52.5
Completeness [%]97.698.8
Redundancy6.76.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP4.5294.215% PEG 4000, 0.1 M Sodium acetate (pH 4.5)

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