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5C9B

Crystal structure of a retropepsin-like aspartic protease from Rickettsia conorii

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]100
Detector technologyCCD
Collection date2012-10-20
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)0.9825
Spacegroup nameP 32 2 1
Unit cell lengths101.985, 101.985, 127.063
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution47.370 - 2.400
R-factor0.20206
Rwork0.199
R-free0.26222
RMSD bond length0.016
RMSD bond angle1.819
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareSOLVE
Refinement softwareREFMAC (5.7.0032)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.440
High resolution limit [Å]2.4002.400
Rmerge0.0540.419
Number of reflections28761
<I/σ(I)>31.272.67
Completeness [%]87.633.6
Redundancy5.63.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.829324% PEG4000, 0.2 M lithium sulfate, pH 5.8

219869

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