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3WCW

The structure of a deoxygenated 400 kda hemoglobin provides a more accurate description of the cooperative mechanism of giant hemoglobins: MG bound form

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL41XU
Synchrotron siteSPring-8
BeamlineBL41XU
Temperature [K]90
Detector technologyCCD
Collection date2010-11-11
DetectorRAYONIX MX225HE
Wavelength(s)1.0000
Spacegroup nameP 63
Unit cell lengths109.273, 109.273, 195.599
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution43.440 - 2.500
R-factor0.207
Rwork0.207
R-free0.25900
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)3wct
RMSD bond length0.008
RMSD bond angle1.200
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareCNS (1.2)
Refinement softwareCNS (1.2)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.590
High resolution limit [Å]2.5002.500
Number of reflections45675
<I/σ(I)>15.14
Completeness [%]100.099.9
Redundancy5.75.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.529313-18% PEG 3350, 0-5mM Ca acetate/Mg acetate, 100mM HEPES-NaOH, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K

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