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1N3C

Structural and biochemical exploration of a critical amino acid in human 8-oxoguanine glycosylase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsCHESS BEAMLINE A1
Synchrotron siteCHESS
BeamlineA1
Temperature [K]100
Detector technologyCCD
Collection date2001-04-09
DetectorADSC QUANTUM 4
Wavelength(s)0.93
Spacegroup nameP 65 2 2
Unit cell lengths92.255, 92.255, 210.600
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution30.000

*

- 2.700
R-factor0.225
Rwork0.225
R-free0.27000

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ebm
RMSD bond length0.006
RMSD bond angle21.200

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Data reduction softwareHKL-2000
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.870
High resolution limit [Å]2.7002.700
Rmerge0.1370.526
Total number of observations88563

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Number of reflections14671
<I/σ(I)>153.9
Completeness [%]92.690.1
Redundancy6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.4

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4

*

Bruner, S.D., (2000) Nature, 403, 859.

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Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111sodium cacodylate
211calcium acetate
311PEG 8000
412PEG 8000
512calcium acetate
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropTris-HCl20 (mM)
21drop100 (mM)
31dropEDTA1 (mM)
41dropdithiothreitol10 (mM)
51reservoirsodium cacodylate100 (mM)
61reservoircalcium acetate200 (mM)
71reservoirPEG800017-18 (%)

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