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4EGN

The X-ray crystal structure of CYP199A4 in complex with veratric acid

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL17U
Synchrotron siteSSRF
BeamlineBL17U
Temperature [K]100
Detector technologyCCD
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)0.9796
Spacegroup nameP 21 21 21
Unit cell lengths106.534, 143.444, 172.820
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.440 - 2.000
R-factor0.17257
Rwork0.171
R-free0.20747
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4dnz
RMSD bond length0.028
RMSD bond angle2.094
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareCCP4
Refinement softwareREFMAC (5.5.0109)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.070
High resolution limit [Å]2.0002.000
Rmerge0.1000.595
Number of reflections176183
<I/σ(I)>16.63.05
Completeness [%]98.598.5
Redundancy65.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.52930.1M Bis-tris, 1.45M (NH4)2SO4, 0.1M NaCl, 30%(w/v) 1,5-Diaminopentane dihydrochloride, pH 5.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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