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1H66

CRYSTAL STRUCTURE OF HUMAN NAD[P]H-QUINONE OXIDOREDUCTASE CO WITH 2,5-diaziridinyl-3-hydroxyl-6-methyl-1,4-benzoquinone

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X25
Synchrotron siteNSLS
BeamlineX25
Temperature [K]100
Detector technologyCCD
DetectorBRANDEIS CCD
Spacegroup nameP 1
Unit cell lengths56.185, 57.080, 97.323
Unit cell angles77.05, 77.07, 87.22
Refinement procedure
Resolution19.960 - 2.000
R-factor0.199

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Rwork0.256
R-free0.25600

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Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.008
RMSD bond angle22.100

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS (1.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]19.960
High resolution limit [Å]2.000
Rmerge0.091

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Number of reflections73718
Completeness [%]93.883.8

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Redundancy3.9

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Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

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8

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25

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Faig, M., (2000) Proc.Natl.Acad.Sci.USA, 97, 3177.

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein10-15 (mg/ml)
21dropTris-HCl25 (mM)
31dropFAD0.005 (mM)
41reservoirPEG335030 (%)
51reservoirsodium acetate200 (mM)
61reservoirsodium tricine100 (mg/ml)
71reservoirFAD0.012-0.024 (mM)

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PDB entries from 2024-05-15

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