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1QAF

THE ACTIVE SITE BASE CONTROLS COFACTOR REACTIVITY IN ESCHERICHIA COLI AMINE OXIDASE : X-RAY CRYSTALLOGRAPHIC STUDIES WITH MUTATIONAL VARIANTS

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX7.2
Synchrotron siteSRS
BeamlinePX7.2
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1997-06-21
DetectorMARRESEARCH
Spacegroup nameP 21 21 21
Unit cell lengths135.200, 167.000, 79.930
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 2.200
R-factor0.179
Rwork0.176
R-free0.24429
Structure solution methodDIFFERENCE FOURIER
Starting model (for MR)1oac
RMSD bond length0.012
RMSD bond angle0.049
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.300
High resolution limit [Å]2.2002.200
Rmerge0.0660.204
Number of reflections84390

*

<I/σ(I)>8.33.2
Completeness [%]91.673.3
Redundancy2.91.03
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.1315VAPOR DIFFUSION, SITTING DROP PH 7.1, 315 K SODIUM CITRATE, HEPES
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirsodium citrate1.3 (M)
21reservoirHEPES100 (mM)

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