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4HI1

Crystal structure of acylphosphatase C20R mutant from Vibrio cholerae0395

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsENRAF-NONIUS FR591
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2012-07-13
DetectorMAR scanner 345 mm plate
Wavelength(s)1.5418
Spacegroup nameP 1 21 1
Unit cell lengths39.710, 81.300, 40.530
Unit cell angles90.00, 90.52, 90.00
Refinement procedure
Resolution39.708 - 1.964
R-factor0.1907
Rwork0.187
R-free0.24870
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2bjd
RMSD bond length0.011
RMSD bond angle1.328
Data reduction softwareiMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwarePHENIX ((phenix.refine: 1.8_1069))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]39.7082.060
High resolution limit [Å]1.9641.960
Rmerge0.062
Number of reflections17237
<I/σ(I)>12.5
Completeness [%]93.593.5
Redundancy3.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP92931.6M ammonium sulfate, 0.1M bicine pH 9.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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