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3TT9

Crystal structure of the stable degradation fragment of human plakophilin 2 isoform a (PKP2a) C752R variant

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.1
Synchrotron siteBESSY
Beamline14.1
Temperature [K]100
Detector technologyCCD
Collection date2009-05-19
DetectorRAYONIX MX-225
Wavelength(s)0.91841
Spacegroup nameP 21 21 21
Unit cell lengths46.350, 63.038, 74.953
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution33.420 - 1.550
R-factor0.15994
Rwork0.158
R-free0.19231
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1xm9
RMSD bond length0.015
RMSD bond angle1.595
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHASER
Refinement softwareREFMAC (5.5.0066)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]35.0001.590
High resolution limit [Å]1.5501.550
Number of reflections32363
<I/σ(I)>2.87
Completeness [%]99.498.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7293.15reservoir: 22% (w/v) PEG 3350, 75 M malonic acid pH 7.0, protein: 5 mg/mL in 20 mM HEPES, NaOH pH 7.5, 0.1 M NaCl, 3 mM DTT, mix 1:1, VAPOR DIFFUSION, HANGING DROP, temperature 293.15K

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