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4YYT

Human Carbonic Anhydrase II complexed with an inhibitor with a benzenesulfonamide group (5).

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.1
Synchrotron siteBESSY
Beamline14.1
Temperature [K]100
Detector technologyPIXEL
Collection date2013-12-13
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.91841
Spacegroup nameP 1 21 1
Unit cell lengths42.463, 41.703, 72.321
Unit cell angles90.00, 104.33, 90.00
Refinement procedure
Resolution41.142 - 1.070
R-factor0.1441
Rwork0.143
R-free0.16580
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1cni
RMSD bond length0.005
RMSD bond angle1.109
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHASER
Refinement softwarePHENIX ((phenix.refine: 1.8.4_1492))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.130
High resolution limit [Å]1.0701.070
Number of reflections107591
<I/σ(I)>11.62.13
Completeness [%]99.398.9
Redundancy3.193.03
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP2912.5 uL of the protein solution (10 mg/ml hCAII in 50 mM Tris pH 7.8) were mixed with 2.5 uL of the well solution (2.7 M (NH4)SO4, 100 mM Tris, pH 7.8, saturated with p-chloromercurybenzoicacid) and placed as a hanging drop. Crystals appeared after several days. The crystals were soaked in 3.0 M (NH4)SO4, 100 mM Tris, pH 7.8, saturated with the inhibitor, for 1 day.

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