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2J0D

Crystal structure of human P450 3A4 in complex with erythromycin

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-4
Synchrotron siteESRF
BeamlineID14-4
Temperature [K]100
Detector technologyCCD
Collection date2005-07-19
DetectorADSC CCD
Spacegroup nameC 2 2 21
Unit cell lengths67.254, 210.706, 161.246
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 2.750
R-factor0.242
Rwork0.238
R-free0.31500
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1w0e
RMSD bond length0.011
RMSD bond angle1.332
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]29.8002.820
High resolution limit [Å]2.7502.750
Rmerge0.1000.560
Number of reflections30291
<I/σ(I)>16.43.9
Completeness [%]99.9100
Redundancy7.27.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5HANGING DROP CRYSTALLISATION USING 1:1 RATIO OF PROTEIN AT 20-27 MG/ML AGAINST 0.1 M HEPES PH 7-7.5, 0.2 M LITHIUM SULFATE,0.8-1.0 M LITHIUM CHLORIDE AND 30% PEG4000

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