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3MIN

NITROGENASE MOFE PROTEIN FROM AZOTOBACTER VINELANDII, OXIDIZED STATE

Experimental procedure
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL7-1
Synchrotron siteSSRL
BeamlineBL7-1
Temperature [K]90
Detector technologyIMAGE PLATE
Collection date1996-07
DetectorMARRESEARCH
Spacegroup nameP 1 21 1
Unit cell lengths108.000, 131.300, 81.000
Unit cell angles90.00, 110.70, 90.00
Refinement procedure
Resolution30.000 - 2.030
R-factor0.206
Rwork0.206
R-free0.26400
RMSD bond length0.015
RMSD bond angle23.500

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.0)
Refinement softwareX-PLOR (3.98)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.060
High resolution limit [Å]2.0302.030
Rmerge0.0580.162
Total number of observations576617

*

Number of reflections125145
<I/σ(I)>164
Completeness [%]92.077.1
Redundancy4.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Batch method

*

8.5PROTEIN WAS CRYSTALLIZED USING PRECIPITATING SOLUTION OF 30% PEG 4000, 0.2M NA2MO4, 0.1M TRIS PH 8.5 SOAKED IN SOAKED IN SODIUM DITHIONITE, 10MM FINAL CONC.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111PEG800030 (%)
2110.2 (M)
311Tris-HCl0.1 (M)

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