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5IJ6

Crystal structure of Enterococcus faecalis lipoate-protein ligase A (lplA-1) in complex with lipoic acid

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsCLSI BEAMLINE 08ID-1
Synchrotron siteCLSI
Beamline08ID-1
Temperature [K]100
Detector technologyCCD
Collection date2015-10-01
DetectorRAYONIX MX-300
Wavelength(s)0.97949
Spacegroup nameP 21 21 21
Unit cell lengths53.011, 70.912, 106.466
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution39.470 - 2.000
R-factor0.1793
Rwork0.178
R-free0.20700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5iby
RMSD bond length0.012
RMSD bond angle1.174
Data reduction softwareXDS
Data scaling softwareSCALA (3.3.21)
Phasing softwarePHASER (2.5.2)
Refinement softwareREFMAC (5.7.0032)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]39.44039.4402.050
High resolution limit [Å]2.0008.7202.000
Rmerge0.1450.0710.593
Rmeas0.1540.0760.629
Rpim0.0520.0270.208
Total number of observations240100292419150
Number of reflections27879
<I/σ(I)>9.1163.3
Completeness [%]100.099.1100
Redundancy8.67.38.9
CC(1/2)0.9940.9900.918
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.52890.5 UL PROTEIN + 0.5 UL BUFFER (30% PEG 4K, 0.2 M LITHIUM SULFATE, 0.1 M Tris HCl, PH 8.5)

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