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3M98

Crystal structure of human carbonic anhydrase isozyme II with 5-(1H-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE X13
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineX13
Temperature [K]100
Detector technologyCCD
Collection date2009-12-21
DetectorMAR CCD 165 mm
Wavelength(s)0.8120
Spacegroup nameP 1 21 1
Unit cell lengths42.233, 41.112, 72.109
Unit cell angles90.00, 104.05, 90.00
Refinement procedure
Resolution39.810 - 1.500
R-factor0.13976
Rwork0.135
R-free0.18400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3hlj
RMSD bond length0.029
RMSD bond angle2.224
Data reduction softwareMOSFLM
Data scaling softwareSCALA (3.2.19)
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]39.8101.580
High resolution limit [Å]1.5001.500
Rmerge0.0450.324
Number of reflections37890
<I/σ(I)>35.96
Completeness [%]98.097.1
Redundancy9.99.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP291Crystallization buffer was 0.1M sodium BICINE, pH 9.0, 0.2 M ammonium sulfate and 2M sodium malonate, pH 7.0 made from 1M sodium BICINE and 3.4M sodium malonate, vapor diffusion, sitting drop, temperature 291K

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