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2REA

Crystal structures of C2ALPHA-PI3 kinase PX-domain domain indicate conformational change associated with ligand binding.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]105
Detector technologyIMAGE PLATE
Collection date2004-11-04
DetectorRIGAKU RAXIS IV
Wavelength(s)1.5418
Spacegroup nameP 31 2 1
Unit cell lengths56.866, 56.866, 92.995
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution27.190 - 2.500
R-factor0.23454
Rwork0.231
R-free0.31808
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ocs
RMSD bond length0.034
RMSD bond angle2.814
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareEPMR
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.590
High resolution limit [Å]2.5002.500
Rmerge0.0280.107
Number of reflections5731
<I/σ(I)>409
Completeness [%]89.470.9
Redundancy3.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP62930.1M MALEIC ACID/NAOH, 10% GLYCEROL, PH 6.00, VAPOR DIFFUSION, HANGING DROP, TEMPERATURE 293K

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