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2HF2

Domain shifting confirms monomeric structure of Escherichia sugar phosphatase SUPH

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2006-05-03
DetectorRIGAKU RAXIS IV
Wavelength(s)1.5418
Spacegroup nameP 1 21 1
Unit cell lengths38.774, 111.295, 68.802
Unit cell angles90.00, 106.23, 90.00
Refinement procedure
Resolution20.000 - 1.900
R-factor0.2058
Rwork0.204
R-free0.25188
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1rlm
RMSD bond length0.023
RMSD bond angle1.410
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.970
High resolution limit [Å]1.9001.900
Rmerge0.0560.323
Number of reflections42397
<I/σ(I)>13.43.6
Completeness [%]95.673.6
Redundancy74.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP4.529020% PEG8000, 0.1 M SODIUM PHOSPHATE-CITRATE, 10% GLYCEROL, pH 4.50, VAPOR DIFFUSION, SITTING DROP, temperature 290K

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