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2GHC

Conformational mobility in the active site of a heme peroxidase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID23-1
Synchrotron siteESRF
BeamlineID23-1
Temperature [K]100
Detector technologyCCD
Collection date2005-11-08
DetectorADSC QUANTUM 315
Wavelength(s)1.0000
Spacegroup nameP 42 21 2
Unit cell lengths81.909, 81.909, 75.140
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution36.640 - 1.250
R-factor0.18965
Rwork0.189
R-free0.20721
Structure solution methodFOURIER SYNTHESIS
RMSD bond length0.006
RMSD bond angle1.049
Data reduction softwareMOSFLM
Refinement softwareREFMAC (5.2)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]45.8801.320
High resolution limit [Å]1.2501.250
Rmerge0.107
Number of reflections71053
<I/σ(I)>12.83.9
Completeness [%]98.699.9
Redundancy4.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.32730.1 M HEPES, pH 8.3, 2.25 M Lithium Sulphate, VAPOR DIFFUSION, SITTING DROP, temperature 273K

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