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1M1Y

Chemical Crosslink of Nitrogenase MoFe Protein and Fe Protein

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL9-2
Synchrotron siteSSRL
BeamlineBL9-2
Temperature [K]100
Detector technologyCCD
Collection date2001-04-05
DetectorADSC QUANTUM 4
Wavelength(s)1.005
Spacegroup nameP 21 21 21
Unit cell lengths113.267, 214.937, 320.466
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 3.200
R-factor0.279
Rwork0.279
R-free0.33000

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Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.021
RMSD bond angle1.440
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareMOLREP
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0003.290
High resolution limit [Å]3.2003.200
Rmerge0.0850.666

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Total number of observations225603

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Number of reflections105200
<I/σ(I)>131.7
Completeness [%]81.170.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Batch method

*

84

*

PEG 6000, NaCl, Cadaverine, Tris, pH 8.0, LIQUID DIFFUSION, temperature 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111protein33 (mg/ml)
211Tris-HCl40 (mM)pH8.0
311200 (mM)
411MPD20 (%(v/v))
5115 (mM)
612Tris-HCl75 (mM)pH8.0
712cadaverine HCl510 (mM)
812PEG600020.9 (%(w/w))
9122 (mM)

229380

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