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1AL8

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

Experimental procedure
Temperature [K]277
Detector technologyIMAGE PLATE
Collection date1996-04
DetectorMARRESEARCH
Spacegroup nameI 4
Unit cell lengths95.400, 95.400, 93.500
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution8.000 - 2.200
R-factor0.194
Rwork0.194
R-free0.25100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1gox
RMSD bond length0.007
RMSD bond angle23.780

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]100.0002.250
High resolution limit [Å]2.2002.200
Rmerge0.094

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0.369

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Total number of observations237398

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Number of reflections21308
<I/σ(I)>7.93.3
Completeness [%]99.899.9
Redundancy11.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Microdialysis

*

8.3PROTEIN WAS CRYSTALLIZED FROM 50MM TRIS- BUFFER, 0.25 MG/ML FMN, 4% TERTIARY BUTANOL AND 0.5 % JF 5969, PH 8.3. JF 5969 IS A MIXTURE OF SYMPERONIC NPE1800 (33.3G/L), TWEEN 85 (20G/L) IN CYCLOHEXANONE.
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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PDB entries from 2024-07-10

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