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1D7K

CRYSTAL STRUCTURE OF HUMAN ORNITHINE DECARBOXYLASE AT 2.1 ANGSTROMS RESOLUTION

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsCHESS BEAMLINE A1
Synchrotron siteCHESS
BeamlineA1
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1996-01-15
DetectorFUJI
Spacegroup nameP 21 21 21
Unit cell lengths61.680, 107.450, 139.710
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.500 - 2.100
Rwork0.212
R-free0.28800
RMSD bond length0.016
RMSD bond angle2.500
Data reduction softwareDENZO
Data scaling softwareCCP4 ((SCALA))
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.160
High resolution limit [Å]2.1002.090
Rmerge0.0680.363
Total number of observations223151

*

Number of reflections53656
<I/σ(I)>10.1
Completeness [%]96.497.5
Redundancy43.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1unknown

*

7.528920% PEG 3350, 0.2M NaCl, 5mM DTT, 0.1M Tris-HCl, pH 7.5, VAPOR DIFFUSION, temperature 16K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111protein20 (mg/ml)
212PEG335020 (%(w/v))
312Tris-HCl0.1 (M)
4120.2 (M)

218853

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