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1FN7

COUPLING OF DAMAGE RECOGNITION AND CATALYSIS BY A HUMAN BASE-EXCISION DNA REPAIR PROTEIN

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Detector technologyCCD
Collection date2000-03-07
DetectorSBC-1
Spacegroup nameP 65 2 2
Unit cell lengths92.113, 92.113, 211.014
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution29.850 - 2.600
R-factor0.221
Rwork0.221
R-free0.27000
RMSD bond length0.006
RMSD bond angle20.700

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0002.690
High resolution limit [Å]2.6002.540
Rmerge0.0730.352
Total number of observations83683

*

Number of reflections17653
<I/σ(I)>14.3
Completeness [%]96.699.8
Redundancy4.743.15
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7.4

*

277100 mM sodium cacodylate pH 6.5, 200 mM calcium acetate, 16-18% PEG, VAPOR DIFFUSION, HANGING DROP, temperature 277K
Crystallization Reagents
IDcrystal IDsolution IDreagent nameconcentrationdetails
111sodium cacodylate
211calcium acetate
311PEG
412PEG
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropTris-HCl10 (mM)
21drop50 (mM)
31dropEDTA1 (mM)
41dropbeta-mercaptoethanol5 (mM)
51reservoirsodium cacodylate100 (mM)
61reservoircalcium acetate200 (mM)
71reservoirPEG800016-18 (%)

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PDB entries from 2024-09-18

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