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4CHQ

Interrogating HIV integrase for compounds that bind- a SAMPL challenge

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX1
Synchrotron siteAustralian Synchrotron
BeamlineMX1
Temperature [K]100
Detector technologyCCD
Collection date2008-12-13
DetectorADSC CCD
Spacegroup nameP 31
Unit cell lengths71.573, 71.573, 66.826
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution31.540 - 1.950
R-factor0.18163
Rwork0.180
R-free0.20329
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)PDB ENTRRY 3ZSQ
RMSD bond length0.006
RMSD bond angle1.216
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.7.0032)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]62.0002.060
High resolution limit [Å]1.9501.950
Rmerge0.0800.580
Number of reflections27833
<I/σ(I)>14.42.7
Completeness [%]99.798
Redundancy5.75.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
15.5THE PROTEIN WAS CONCENTRATED TO 5.5 MG/ML IN 40 MM TRIS PH 8.0, 250 MM NACL, 30 MM MGCL2, 5 MM DTT AND SET UP IN A 1:1 RATIO WITH 1.6 TO 2.0 M AMMONIUM SULFATE, 100 MM SODIUM ACETATE BUFFER PH 5.0 TO 5.5.

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