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5OCX

Crystal structure of ACPA E4 in complex with CII-C-13-CIT

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I02
Synchrotron siteDiamond
BeamlineI02
Temperature [K]100
Detector technologyPIXEL
Collection date2016-01-28
DetectorDECTRIS PILATUS 6M-F
Wavelength(s)0.9795
Spacegroup nameP 1 21 1
Unit cell lengths38.716, 99.602, 51.877
Unit cell angles90.00, 101.88, 90.00
Refinement procedure
Resolution45.230 - 1.750
R-factor0.17812
Rwork0.176
R-free0.21231
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4m1q 3lmj
RMSD bond length0.009
RMSD bond angle1.428
Data reduction softwarexia2
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0158)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]45.2301.780
High resolution limit [Å]1.7501.750
Rmerge0.0830.584
Rpim0.0760.539
Number of reflections376601896
<I/σ(I)>7.51.3
Completeness [%]97.390
Redundancy3.12.7
CC(1/2)0.9940.606
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP29320% (w/v) PEG3350, 0.2 M ammonium citrate dibasic

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