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3EFI

Carbonic anhydrase activators: Kinetic and X-ray crystallographic study for the interaction of d- and l-tryptophan with the mammalian isoforms I-XIV

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSEALED TUBE
Source detailsOXFORD DIFFRACTION ENHANCED ULTRA
Temperature [K]100
Detector technologyCCD
Collection date2008-04-01
DetectorOXFORD SAPPHIRE CCD
Wavelength(s)1.5418
Spacegroup nameP 1 21 1
Unit cell lengths42.070, 41.320, 72.050
Unit cell angles90.00, 104.40, 90.00
Refinement procedure
Resolution10.380 - 1.750
R-factor0.19063
Rwork0.189
R-free0.22243
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ca2
RMSD bond length0.017
RMSD bond angle1.746
Data reduction softwareCrysalisPro (Oxford Diffraction2006)
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.860
High resolution limit [Å]1.7501.750
Number of reflections24484
<I/σ(I)>15.142.9
Completeness [%]99.099
Redundancy3.62.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP27750mM Tris.HCl pH 7.7-7.8, 2mM sodium 4-(hydroxymercury)benzoate, VAPOR DIFFUSION, HANGING DROP, temperature 277K

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