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1B3A

TOTAL CHEMICAL SYNTHESIS AND HIGH-RESOLUTION CRYSTAL STRUCTURE OF THE POTENT ANTI-HIV PROTEIN AOP-RANTES

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X9B
Synchrotron siteNSLS
BeamlineX9B
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1998-05
DetectorMAR scanner 345 mm plate
Spacegroup nameP 21 21 21
Unit cell lengths23.635, 56.307, 94.030
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 1.600
R-factor0.167

*

R-free0.24060
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.008
RMSD bond angle0.024
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareAMoRE
Refinement softwareSHELXL-97
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.660
High resolution limit [Å]1.6001.600
Rmerge0.0430.196
Total number of observations74936

*

Number of reflections17338
<I/σ(I)>31.87.5
Completeness [%]99.8100
Redundancy4.34.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

4.620

*

pH 4.6
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropsodium acetate10 (mM)
21dropprotein15 (mg/ml)
31reservoirammonium sulfate0.1 (M)
41reservoirsodium succinate225 (mM)
51reservoir2-(N-morpholino)ethanesulfonic acid275 (mM)
61reservoirethanol15 (%)

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