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4ETL

Crystallographic structure of phenylalanine hydroxylase from Chromobacterium violaceum F258A mutation

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 23-ID-B
Synchrotron siteAPS
Beamline23-ID-B
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2012-03-05
DetectorMAR scanner 300 mm plate
Wavelength(s)1.033
Spacegroup nameP 1
Unit cell lengths36.780, 38.553, 48.044
Unit cell angles76.47, 73.00, 85.36
Refinement procedure
Resolution22.680 - 1.490
R-factor0.16727
Rwork0.165
R-free0.21421
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ltu
RMSD bond length0.007
RMSD bond angle1.248
Data reduction softwareHKL-3000
Data scaling softwareHKL-3000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.6.0117)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.520
High resolution limit [Å]1.4901.490
Rmerge0.059
Number of reflections36922
<I/σ(I)>20.1
Completeness [%]92.059.7
Redundancy3.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP72930.1M Na-HEPES, 0.001M Magnesium chloride hexahydrate, 0.005M Nickel (II) chloride hexahydrate, 15% w/v PEG 3,350, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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