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5FHY

Crystal structure of FliD (HAP2) from Pseudomonas aeruginosa PAO1

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 23-ID-B
Synchrotron siteAPS
Beamline23-ID-B
Temperature [K]100
Detector technologyCCD
Collection date2015-07-08
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)1.0332
Spacegroup nameP 6
Unit cell lengths124.741, 124.741, 107.010
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution62.371 - 2.201
R-factor0.251
Rwork0.249
R-free0.28670
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)low resolution SeMet protein
RMSD bond length0.004
RMSD bond angle0.955
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwarePHENIX (1.9_1692)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]62.4002.280
High resolution limit [Å]2.2002.200
Rmerge0.0853.702
Number of reflections47974
<I/σ(I)>17.150.55
Completeness [%]99.999.2
Redundancy7.77.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.5298Crystallized in 0.8 M NaK Tartrate, 0.1 M Hepes pH 7.5 using random matrix microseed screening

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