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4KSB

Structures of P-glycoprotein reveal its conformational flexibility and an epitope on the nucleotide-binding domain

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL11-1
Synchrotron siteSSRL
BeamlineBL11-1
Temperature [K]100
Detector technologyPIXEL
Collection date2012-12-07
DetectorPSI PILATUS 6M
Wavelength(s)1
Spacegroup nameP 21 21 21
Unit cell lengths87.400, 138.650, 185.130
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution92.565 - 3.800
R-factor0.3247
Rwork0.323
R-free0.35660
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.004
RMSD bond angle0.869
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareCNS
Refinement softwarePHENIX ((phenix.refine: 1.8.2_1309))
Data quality characteristics
 Overall
Low resolution limit [Å]92.592
High resolution limit [Å]3.800
Number of reflections22815
Completeness [%]95.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP727725-29.5% w/v PEG 600, 50 mM LiSO4, 10 mM EDTA, 100 mM Hepes, pH 7, VAPOR DIFFUSION, SITTING DROP, temperature 277K

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