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1G6O

CRYSTAL STRUCTURE OF THE HELICOBACTER PYLORI ATPASE, HP0525, IN COMPLEX WITH ADP

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Wavelength(s)0.9792
Spacegroup nameP 63 2 2
Unit cell lengths112.620, 112.620, 234.830
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution30.000 - 2.500
R-factor0.224
Rwork0.224
R-free0.28900
Structure solution methodSAD
RMSD bond length0.012
RMSD bond angle1.600
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.000

*

2.590
High resolution limit [Å]2.5002.500
Rmerge0.1020.158
Total number of observations137723

*

Number of reflections27352
<I/σ(I)>10.7
Completeness [%]88.871.4
Redundancy54
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7298PEG 1000, calcium acetate, glycerol, ADP-Mg, Tris-HCl, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 298.0K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein30 (mg/ml)
21reservoirTris-HCl100 (mM)
31reservoirPEG100019-21 (%)
41reservoircalcium acetate0.2 (M)
51reservoirglycerol15 (%)

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PDB entries from 2025-12-10

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