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1F8W

CRYSTAL STRUCTURE OF NADH PEROXIDASE MUTANT: R303M

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL7-1
Synchrotron siteSSRL
BeamlineBL7-1
Temperature [K]110
Detector technologyIMAGE PLATE
Collection date1996-08-08
DetectorMARRESEARCH
Spacegroup nameI 41 2 2
Unit cell lengths155.180, 155.180, 189.410
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution50.000 - 2.450
R-factor0.196

*

Rwork0.196
R-free0.23400
RMSD bond length0.016
RMSD bond angle3.000
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]99.000
High resolution limit [Å]2.4502.450
Rmerge0.048

*

0.363
Total number of observations60231

*

Number of reflections36615
<I/σ(I)>9.52.6
Completeness [%]85.870.9

*

Redundancy5.43.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

7.22962% PEG 400, 2.0 M (NH4)2SO4, 100 mM Na Hepes, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 296K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropPEG4002-8 (%)
21dropammonium sulfate1.6-1.9 (M)
31dropsodium HEPES0.1 (M)
41dropprotein7.5-10 (mg/ml)

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