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2GK2

Crystal structure of the N terminal domain of human CEACAM1

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]100
Detector technologyCCD
Collection date2005-06-26
DetectorMARMOSAIC 300 mm CCD
Wavelength(s)1.00
Spacegroup nameP 63
Unit cell lengths86.200, 86.200, 62.000
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution50.000 - 2.200
R-factor0.213
Rwork0.210
R-free0.25800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1l6z
RMSD bond length0.013
RMSD bond angle1.537
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.280
High resolution limit [Å]2.2002.200
Rmerge0.0670.736
Number of reflections13366
<I/σ(I)>38.82
Completeness [%]99.696.9
Redundancy10.56.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.529416% (w/v) polyethylene glycol mono methyl ether 2000, 100 mM Tris, and 5 mM nickel chloride, pH 8.5, VAPOR DIFFUSION, HANGING DROP, temperature 294K

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