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2C8V

Insights into the role of nucleotide-dependent conformational change in nitrogenase catalysis: Structural characterization of the nitrogenase Fe protein Leu127 deletion variant with bound MgATP

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL9-2
Synchrotron siteSSRL
BeamlineBL9-2
Temperature [K]93
Detector technologyCCD
Collection date2002-12-20
DetectorMARRESEARCH
Spacegroup nameC 2 2 21
Unit cell lengths70.900, 133.300, 61.500
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution8.000 - 2.500
R-factor0.2381
Rwork0.238
R-free0.27930
Structure solution methodOTHER
RMSD bond length0.010
RMSD bond angle2.520
Data reduction softwareBlu-Ice
Data scaling softwareMOSFLM
Phasing softwareX-PLOR
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]40.000
High resolution limit [Å]2.5002.500
Rmerge0.0860.079
Number of reflections20818
<I/σ(I)>4.15.1
Completeness [%]97.899.9
Redundancy44.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1824% POLY(ETHYLENE GLYCOL), MW 4000, 0.16 M MGCL2, TRISHYDROCHLORIC ACID, PH 8.5, 20% GLYCEROL, AND 1MM SODIUM DITHIONITE

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