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5C9F

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

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]100
Detector technologyCCD
Collection date2013-12-14
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)1.000
Spacegroup nameP 21 21 21
Unit cell lengths50.102, 94.153, 118.636
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution40.000 - 2.000
R-factor0.20034
Rwork0.199
R-free0.25452
RMSD bond length0.015
RMSD bond angle1.725
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwarePHASER
Refinement softwareREFMAC (5.7.0032)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.030
High resolution limit [Å]2.0002.000
Rmerge0.510
Number of reflections36685
<I/σ(I)>30.561.74
Completeness [%]94.964
Redundancy7.43.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.829324% PEG4000, 0.2 M lithium sulfate, pH 5.8

219869

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