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4J4Q

Crystal structure of active conformation of GPCR opsin stabilized by octylglucoside

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.2
Synchrotron siteBESSY
Beamline14.2
Temperature [K]100
Detector technologyCCD
Collection date2010-05-06
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)0.91841
Spacegroup nameH 3 2
Unit cell lengths241.265, 241.265, 109.561
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution33.460 - 2.650
R-factor0.21794
Rwork0.217
R-free0.23032
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3dqb
RMSD bond length0.010
RMSD bond angle1.278
Data reduction softwareXDS
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.5.0072)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]33.4602.790
High resolution limit [Å]2.6502.650
Rmerge0.0550.421
Number of reflections35401
<I/σ(I)>17.33.3
Completeness [%]100.0100
Redundancy4.44.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.6277AMMONIUM SULFATE, pH 5.6, VAPOR DIFFUSION, HANGING DROP, temperature 277K

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