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7A11

LppS with covalent adduct derived from 1E

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsMAX IV BEAMLINE BioMAX
Synchrotron siteMAX IV
BeamlineBioMAX
Temperature [K]100
Detector technologyPIXEL
Collection date2019-03-27
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.82656
Spacegroup nameP 1 21 1
Unit cell lengths50.563, 74.552, 67.253
Unit cell angles90.00, 111.78, 90.00
Refinement procedure
Resolution38.000 - 1.650
R-factor0.166
Rwork0.164
R-free0.20700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5lbg
RMSD bond length0.019
RMSD bond angle1.810
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwareMOLREP
Refinement softwareREFMAC (5.8.0103)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]39.7301.680
High resolution limit [Å]1.6501.650
Rmerge0.0590.931
Number of reflections558022746
<I/σ(I)>14.21.8
Completeness [%]100.0100
Redundancy7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.25293Well solution: 0.1 M Na-Citrate pH 4.25 / 17.5% PEG 6K JM12 was added to the soaking solution at 4 mM concentration. In the soaking drop, Citrate is replaced by Acetate (0.3 M) 150 mM NaCl 0.1 M Bis-Tris pH 6.2 0.3 M Na-Acetate pH 5.2 25% PEG 6K PEG 6K INCREASED to 25% FOR CRYO-PROTECTION

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