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1F1U

CRYSTAL STRUCTURE OF HOMOPROTOCATECHUATE 2,3-DIOXYGENASE FROM ARTHROBACTER GLOBIFORMIS (NATIVE, LOW TEMPERATURE)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]200
Detector technologyCCD
Collection date1998-08-29
DetectorCUSTOM-MADE
Spacegroup nameC 1 2 1
Unit cell lengths137.800, 59.040, 102.250
Unit cell angles90.00, 119.00, 90.00
Refinement procedure
Resolution20.000 - 1.500
R-factor0.162
Rwork0.162
R-free0.18500
RMSD bond length0.022
RMSD bond angle2.100
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.630
High resolution limit [Å]1.5001.510
Rmerge0.081

*

0.271
Number of reflections111428
<I/σ(I)>22
Completeness [%]96.993.4

*

Redundancy3.0

*

2.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Batch method

*

6.5

*

18

*

Peg 8000, Mg Acetate Na cacodylate. Data was collected with added glycerol as a cryoprotectant., pH 6.8, Batch crystallization, temperature 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111protein100 (mg/ml)
212PEG80006-10 (%)
312magnesium acetate0.2 (M)
412sodium cacodylate100 (mM)pH6.5

219140

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