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1O8U

The 2 Angstrom Structure of 6-Oxo Camphor Hydrolase: New Structural Diversity in the Crotonase Superfamily

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE BM14
Synchrotron siteESRF
BeamlineBM14
Temperature [K]120
Detector technologyCCD
Collection date2001-09-15
DetectorADSC CCD
Wavelength(s)0.97900,0.97937,0.88560
Spacegroup nameP 1 21 1
Unit cell lengths78.950, 130.410, 81.320
Unit cell angles90.00, 114.16, 90.00
Refinement procedure
Resolution30.000

*

- 2.000
R-factor0.149
Rwork0.147
R-free0.19000
Structure solution methodMAD
RMSD bond length0.017
RMSD bond angle1.630
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareSOLVE
Refinement softwareREFMAC (5.1.24)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.030
High resolution limit [Å]2.0002.000
Rmerge0.0430.157
Number of reflections95532
<I/σ(I)>25.87.1
Completeness [%]99.797
Redundancy2.4

*

3.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7

*

VAPOUR DIFFUSION HANGING DROP PROTEIN SOLUTION: 10 MG/ML IN 50 MM TRIS-HCL PH 7.0, 1 MM DTT, 20 MICROMOLAR PMSF RESERVOIR: 0.1 M SODIUM ACETATE,0.2 M AMMONIUM SULPHATE, 28% (V/V) PEG 4K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10 (mg/ml)
21dropTris-HCl50 (mM)pH7.0
31dropdithiothreitol1 (mM)
41dropPMSF20000 (mM)
51reservoirsodium acetate0.1 (M)pH4.5
61reservoirammonium sulfate0.2 (M)
71reservoirPEG400028 (%(v/v))

218853

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