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3E04

Crystal structure of human fumarate hydratase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSLS BEAMLINE X10SA
Synchrotron siteSLS
BeamlineX10SA
Temperature [K]100
Detector technologyCCD
Collection date2008-06-21
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)1.000
Spacegroup nameP 32 2 1
Unit cell lengths188.483, 188.483, 114.632
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution25.000 - 1.950
R-factor0.19728
Rwork0.197
R-free0.24408
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1yfm
RMSD bond length0.015
RMSD bond angle1.419
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.060
High resolution limit [Å]1.9501.950
Rmerge0.140
Number of reflections168629
<I/σ(I)>9.72
Completeness [%]99.396.8
Redundancy6.25
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.529820% PEG 3350, 10% ethanediol, 0.2 M sodium acetate, 0.1 M bis-tris propane, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 298K

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