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3B4F

Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide with twelve mammalian isoforms: kinetic and X-Ray crystallographic studies

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSEALED TUBE
Source detailsOXFORD DIFFRACTION ENHANCE ULTRA
Temperature [K]100
Detector technologyCCD
Collection date2007-09-01
DetectorOXFORD SAPPHIRE CCD
Wavelength(s)1.5418
Spacegroup nameP 1 21 1
Unit cell lengths42.000, 41.350, 72.340
Unit cell angles90.00, 104.35, 90.00
Refinement procedure
Resolution20.000 - 1.890
R-factor0.1983
Rwork0.196
R-free0.23862
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ca2
RMSD bond length0.009
RMSD bond angle1.543
Data reduction softwareCrysalisPro (Oxford Diffraction2006)
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.970
High resolution limit [Å]1.8901.890
Number of reflections19119
Completeness [%]99.0
Redundancy4.63
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.7277Tris HCl pH 7.7-7.8 , sodium 4-(hydroxymercury)benzoate , VAPOR DIFFUSION, HANGING DROP, temperature 277K

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