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1H2R

THREE-DIMENSIONAL STRUCTURE OF NI-FE HYDROGENASE FROM DESULFIVIBRIO VULGARIS MIYAZAKI F IN THE REDUCED FORM AT 1.4 A RESOLUTION

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSPRING-8 BEAMLINE BL41XU
Synchrotron siteSPring-8
BeamlineBL41XU
Temperature [K]280
Detector technologyIMAGE PLATE
Spacegroup nameP 21 21 21
Unit cell lengths100.440, 126.860, 66.680
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution6.000 - 1.400
R-factor0.218
Rwork0.218
R-free0.25400
Structure solution methodD-FOURIER
Starting model (for MR)1h2a
RMSD bond length0.012
RMSD bond angle1.960
Data reduction softwareDENZO
Data scaling softwareCCP4 ((SCALA))
Phasing softwareMLPHARE ((CCP4))
Refinement softwareX-PLOR
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.460
High resolution limit [Å]1.4001.400
Rmerge0.0480.380
Total number of observations1453748

*

Number of reflections155198
Completeness [%]91.685.8

*

Redundancy9.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Microdialysis

*

7.4

*

Higuchi, Y., (1987) J.Biol.Chem., 262, 2823.

*

Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111protein40 (mg/ml)
211Tris-HCl25 (mM)
31120 (mM)
412PEG20 (%(w/v))
512sodium citrate20 (%(w/v))
612ammonium sulfate40 (%sat)
712ethanol40 (%(v/v))
812MPD40 (%(v/v))or 1M NaCl

220113

PDB entries from 2024-05-22

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