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1CVU

CRYSTAL STRUCTURE OF ARACHIDONIC ACID BOUND TO THE CYCLOOXYGENASE ACTIVE SITE OF COX-2

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU300
Temperature [K]130
Detector technologyIMAGE PLATE
Collection date1998-10-08
DetectorRIGAKU RAXIS IV
Spacegroup nameI 2 2 2
Unit cell lengths181.036, 133.960, 124.834
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution35.000 - 2.400
R-factor0.206

*

Rwork0.204
R-free0.23500
RMSD bond length0.010
RMSD bond angle24.400
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR
Refinement softwareX-PLOR (3.851)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]35.0002.490
High resolution limit [Å]2.4002.400
Rmerge0.0780.241
Total number of observations212739

*

Number of reflections58608

*

<I/σ(I)>9.6
Completeness [%]98.897.8
Redundancy3.62.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP818

*

Stevens, A.M., (1999) J. Cryst. Growth., 196, 350.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein5 (mg/ml)
101reservoir5-280 (mM)
111reservoirEPPS50 (mM)pH8.0
21dropsodium phosphate10 (mM)
31drop0.005 (%)
41drop50 (mM)
51dropbeta-OG0.9 (%)
61dropMMP5508.1-14.4 (%)
71drop2.25-126 (mM)
81dropEPPS22.5 (mM)
91reservoirMMP55018-32 (%)

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