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1AL7

THREE-DIMENSIONAL STRUCTURES OF GLYCOLATE OXIDASE WITH BOUND ACTIVE-SITE INHIBITORS

Experimental procedure
Temperature [K]277
Detector technologyIMAGE PLATE
Collection date1994-10
DetectorRIGAKU RAXIS II
Spacegroup nameI 4 2 2
Unit cell lengths148.100, 148.100, 136.500
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution8.000 - 2.600
R-factor0.18
Rwork0.180
R-free0.24200
Structure solution methodDIFFERENCE FOURIER
RMSD bond length0.007
RMSD bond angle22.952

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Data reduction softwareDENZO
Data scaling softwareCCP4
Phasing softwareX-PLOR
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]100.0002.680
High resolution limit [Å]2.6002.600
Rmerge0.0850.206
Total number of observations48698

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Number of reflections20291
<I/σ(I)>6.993.1
Completeness [%]87.174.4
Redundancy2.41.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Microdialysis

*

8.3PROTEIN WAS CRYSTALLISED FROM 50MM TRIS-BUFFER PH 8.3, 0.25 MG/ML FMN, 4% TERTIARY BUTANOL, SATURATED WITH THE INHIBITOR.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111protein20 (mg/ml)
211Tris-HCl0.05 (M)
311GOX0.5 (mg/ml)
411FMN0.25 (mg/ml)
511JF59690.5 (%)
612tertiary butanol5 (%(v/v))

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