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6EFV

The NADPH-dependent sulfite reductase flavoprotein adopts an extended conformation that is unique to this diflavin reductase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-BM
Synchrotron siteAPS
Beamline22-BM
Temperature [K]100
Detector technologyCCD
Collection date2018-02-17
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)1.000
Spacegroup nameP 21 21 21
Unit cell lengths60.483, 99.739, 103.533
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution45.947 - 2.341
R-factor0.1717
Rwork0.167
R-free0.23400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ddg
RMSD bond length0.007
RMSD bond angle0.867
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX ((1.11.1_2575: ???))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]45.9472.380
High resolution limit [Å]2.3412.341
Rmeas0.0920.259
Rpim0.0340.102
Number of reflections270361320
<I/σ(I)>10.28.2
Completeness [%]99.9100
Redundancy7.36.4
CC(1/2)0.9970.969
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP10.52981.8 M Ammonium Sulfate, 100 mM Lithium Sulfate, 100 mM CAPS pH 10.5.

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