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4CES

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 date2009-09-18
DetectorADSC CCD
Spacegroup nameP 31
Unit cell lengths71.104, 71.104, 66.665
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution35.560 - 1.850
R-factor0.17062
Rwork0.169
R-free0.19660
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3zsq
RMSD bond length0.014
RMSD bond angle1.395
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASER
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]61.6001.950
High resolution limit [Å]1.8501.850
Rmerge0.0800.310
Number of reflections32198
<I/σ(I)>15.55
Completeness [%]100.0100
Redundancy5.55.6
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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