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3D0N

Crystal structure of human carbonic anhydrase XIII

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsELETTRA BEAMLINE 5.2R
Synchrotron siteELETTRA
Beamline5.2R
Temperature [K]100
Detector technologyCCD
Collection date2007-06-01
DetectorMAR CCD 165 mm
Wavelength(s)0.999882
Spacegroup nameP 1 21 1
Unit cell lengths57.780, 58.210, 72.120
Unit cell angles90.00, 92.36, 90.00
Refinement procedure
Resolution20.000 - 1.550
Rwork0.168
R-free0.18800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ca2
RMSD bond length0.006
RMSD bond angle1.400
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.610
High resolution limit [Å]1.5501.550
Number of reflections68200
<I/σ(I)>21.33.8
Completeness [%]98.190.3
Redundancy3.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.629330% PEG 4000, 0.2 M ammonium acetate, 0.1 M sodium acetate pH 4.6, VAPOR DIFFUSION, HANGING DROP, temperature 293K

220113

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