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4BGC

T1 domain of the renal potassium channel Kv1.3

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSLS BEAMLINE X10SA
Synchrotron siteSLS
BeamlineX10SA
Temperature [K]100
Detector technologyCCD
Collection date2005-04-18
DetectorMARRESEARCH
Spacegroup nameI 4
Unit cell lengths59.740, 59.740, 62.330
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution18.970 - 1.200
R-factor0.16499
Rwork0.163
R-free0.20463
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1qdw
RMSD bond length0.028
RMSD bond angle2.205
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]45.0001.300
High resolution limit [Å]1.2001.200
Rmerge0.0500.160
Number of reflections33942
<I/σ(I)>178.6
Completeness [%]99.298.5
Redundancy3.73
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
16.5WE WANTED TO USE THE PROTEIN IN 150 MM POTASSIUM PHOSPHATE BUFFER PH 6.5 IN 5 MM NMR TUBES FOR CHARACTERIZATION USING NMR SPECTROSCOPY. DURING TESTING, WE OBSERVED THE FORMATION OF CRYSTALS IN THE NMR TUBES. AN INITIAL TEST OF THE CRYSTALS SHOWED AN EXCELLENT DIFFRACTION PATTERN, SO WE DECIDED TO CONTINUE WITH CRYSTALLIZATION OPTIMIZATION IN NMR TUBES, RESULTING IN VERY GOOD CRYSTALS

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