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2O72

Crystal Structure Analysis of human E-cadherin (1-213)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2003-08-03
DetectorMAR scanner 345 mm plate
Wavelength(s)1.0000
Spacegroup nameC 1 2 1
Unit cell lengths137.341, 41.077, 59.542
Unit cell angles90.00, 111.15, 90.00
Refinement procedure
Resolution39.100 - 2.000
R-factor0.193
Rwork0.191
R-free0.23400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1edh
RMSD bond length0.014
RMSD bond angle1.445
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]39.1002.030
High resolution limit [Å]2.0002.000
Rmerge0.0730.323
Number of reflections20837
<I/σ(I)>9.32.5
Completeness [%]98.077.8
Redundancy6.82.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.527710% PEG 8000, 0.2M calcium chloride, 5% DMSO, 0.1M Hepes, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 4K, temperature 277K

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