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2YX6

Crystal structure of PH0822

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL26B1
Synchrotron siteSPring-8
BeamlineBL26B1
Temperature [K]100
Detector technologyCCD
Collection date2006-10-29
DetectorRIGAKU JUPITER 210
Wavelength(s)1.0
Spacegroup nameC 1 2 1
Unit cell lengths94.932, 99.877, 48.812
Unit cell angles90.00, 112.33, 90.00
Refinement procedure
Resolution20.000 - 2.000
R-factor0.21666
Rwork0.214
R-free0.26242
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1o13
RMSD bond length0.021
RMSD bond angle1.871
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareCNS
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.090
High resolution limit [Å]2.0002.000
Rmerge0.0670.123
Number of reflections21963
<I/σ(I)>15.86574.51497
Completeness [%]77.440.6
Redundancy2.757821.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.529320% PEG8000, 0.01M imidazole, 0.01M adenosine-5-triphosphate disodium salt, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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