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3E1I

Crystal Structure of BbetaD432A Variant Fibrinogen Fragment D with the Peptide Ligand Gly-His-Arg-Pro-amide

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]100
Detector technologyCCD
Collection date2005-08-18
DetectorMAR CCD 165 mm
Wavelength(s)0.97625
Spacegroup nameP 21 21 21
Unit cell lengths54.476, 146.596, 228.960
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution49.210 - 2.300
R-factor0.21573
Rwork0.214
R-free0.24154
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1lt9
RMSD bond length0.008
RMSD bond angle1.079
Data reduction softwareHKL-2000
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]2.1502.150
Number of reflections82662
<I/σ(I)>29.53.4
Completeness [%]83.080.5
Redundancy6.75.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.527750 mM Tris, 12.5 mM calcium chloride, 12% PEG 3350, 2 mM sodium azide, pH 8.5, VAPOR DIFFUSION, SITTING DROP, temperature 277K

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