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3O4W

Crystal structure of dimeric KlHxk1 in crystal form IV

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.2
Synchrotron siteBESSY
Beamline14.2
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2005-02-10
DetectorMAR scanner 345 mm plate
Wavelength(s)0.9537
Spacegroup nameP 1 21 1
Unit cell lengths73.710, 91.990, 92.580
Unit cell angles90.00, 110.92, 90.00
Refinement procedure
Resolution29.200 - 1.610
R-factor0.16992
Rwork0.169
R-free0.21996
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3o08
RMSD bond length0.023
RMSD bond angle2.094
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareAMoRE
Refinement softwareREFMAC (5.5.0109)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0001.650
High resolution limit [Å]1.6101.610
Number of reflections129734
<I/σ(I)>18.53.2
Completeness [%]87.098.7
Redundancy5.33.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP9.52921MICROL RESERVOIR + 1MICROL PROTEIN, RESERVOIR: 2.5M AMMONIA SULFATE, 0.1M CHES PH 9.5, PROTEIN: 10MG/ML KLHXK1, 10MM TRIS PH 7.4, 1MM EDTA, 1MM DTT, 0.5MM PMSF, VAPOR DIFFUSION, HANGING DROP, temperature 292K

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