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3SM2

The crystal structure of XMRV protease complexed with Amprenavir

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]100
Detector technologyCCD
Collection date2011-01-01
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)1.000
Spacegroup nameP 21 21 21
Unit cell lengths46.572, 65.099, 69.161
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution27.770 - 1.750
R-factor0.19062
Rwork0.188
R-free0.23444
Structure solution methodFOURIER SYNTHESIS
RMSD bond length0.012
RMSD bond angle1.472
Data reduction softwareHKL-3000
Data scaling softwareHKL-3000
Phasing softwareREFMAC
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0001.810
High resolution limit [Å]1.7501.750
Number of reflections21645
<I/σ(I)>18.932.1
Completeness [%]99.296.2
Redundancy5.84.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.752933.5 M NaFormate, pH 4.75, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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