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1JRL

Crystal structure of E. coli Lysophospholiase L1/Acyl-CoA Thioesterase I/Protease I L109P mutant

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSRRC BEAMLINE BL17B2
Synchrotron siteNSRRC
BeamlineBL17B2
Temperature [K]133
Detector technologyIMAGE PLATE
DetectorMAC Science DIP-2030
Wavelength(s)1.12720
Spacegroup nameP 43 21 2
Unit cell lengths50.011, 50.011, 169.718
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution24.620 - 1.950
Rwork0.195
R-free0.22900
Structure solution methodMIR
RMSD bond length0.005
RMSD bond angle1.200
Data reduction softwareXPRESS
Data scaling softwareSCALEPACK
Phasing softwareSHARP
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]24.6201.960
High resolution limit [Å]1.9301.930
Rmerge0.0420.384
Number of reflections15859
<I/σ(I)>19.35
Completeness [%]96.295.2
Redundancy7.89
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.52982-[N-morpholino]ethanesulfonic acid, PEGMME 5000, Ammonium sulfate, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K

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