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3O1W

Crystal structure of dimeric KlHxk1 in crystal form III

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.3
Synchrotron siteBESSY
Beamline14.3
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2005-02-10
DetectorMAR scanner 345 mm plate
Wavelength(s)0.8940
Spacegroup nameP 1 21 1
Unit cell lengths60.311, 135.844, 72.591
Unit cell angles90.00, 92.06, 90.00
Refinement procedure
Resolution29.850 - 1.660
R-factor0.16172
Rwork0.161
R-free0.20139
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3o08
RMSD bond length0.026
RMSD bond angle2.141
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC (5.5.0109)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0001.700
High resolution limit [Å]1.6601.660
Number of reflections129723
<I/σ(I)>232.2
Completeness [%]94.595.3
Redundancy5.35.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP9.62921MICROL RESERVOIR + 1MICROL PROTEIN, RESERVOIR: 2.2 M AMMONIA DIHYDROGEN PHOSPHATE, 0.1M CHES PH 9.6, 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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