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2WZ1

STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN SOLUBLE GUANYLATE CYCLASE 1 BETA 3.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I03
Synchrotron siteDiamond
BeamlineI03
Temperature [K]287
Detector technologyCCD
Collection date2009-10-14
DetectorADSC CCD
Spacegroup nameC 2 2 21
Unit cell lengths65.590, 90.380, 140.030
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution37.000 - 1.630
R-factor0.18536
Rwork0.184
R-free0.21922
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3et6
RMSD bond length0.016
RMSD bond angle1.585
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.5.0089)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]37.0001.670
High resolution limit [Å]1.6301.630
Rmerge0.0600.560
Number of reflections49220
<I/σ(I)>9.92.1
Completeness [%]99.399.8
Redundancy3.43.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.5PROTEIN WAS CONCENTRATED TO 12 MG/ML IN PURIFICATION BUFFER (10MM HEPES, 500MM NACL, 5% GLYCEROL, 10% GALACTOSE, 0.5MM TCEP)AND SET UP IN SITTING DROP IN A 1:2 RATIO WITH HAMPTON INDEX SCREEN - B8 (1.4M TRI-SODIUM CITRATE DIHYDRATE, 0.1M HEPES, PH 7.5).

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