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2ZFO

Structure of the partially unliganded met state of 400 kDa hemoglobin: Insights into ligand-induced structural changes of giant hemoglobins

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL26B1
Synchrotron siteSPring-8
BeamlineBL26B1
Temperature [K]90
Detector technologyCCD
Collection date2006-06-29
DetectorRIGAKU JUPITER 210
Wavelength(s)1.0000
Spacegroup nameH 3 2
Unit cell lengths110.960, 110.960, 271.580
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution39.220 - 1.950
Rwork0.169
R-free0.20200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2d2m
RMSD bond length0.010
RMSD bond angle1.300
Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareMOLREP
Refinement softwareCNS (1.2)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.020
High resolution limit [Å]1.9501.950
Number of reflections47042
<I/σ(I)>32.85.8
Completeness [%]99.799.4
Redundancy9.27.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP82937% PEG 10000, 0.2M Tris-HCl (pH 8.0), VAPOR DIFFUSION, HANGING DROP, temperature 293K

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