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7AO3

Crystal structure of CotB2 variant F149L in complex with alendronate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.2
Synchrotron siteBESSY
Beamline14.2
Temperature [K]100
Detector technologyPIXEL
Collection date2017-03-09
DetectorDECTRIS PILATUS3 S 2M
Wavelength(s)0.9184
Spacegroup nameP 1
Unit cell lengths53.580, 57.210, 57.630
Unit cell angles90.80, 116.11, 102.21
Refinement procedure
Resolution38.270 - 1.450
R-factor0.1397
Rwork0.138
R-free0.17760
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6ggj
RMSD bond length0.012
RMSD bond angle1.221
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwarePHENIX (1.18.2_3874)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.490
High resolution limit [Å]1.4501.450
Rmeas0.0591.178
Number of reflections1047297681
<I/σ(I)>15.81.3
Completeness [%]98.897.8
Redundancy55
CC(1/2)0.9990.600
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP8.52910.1 M Tris/HCl pH 8.5 28% (w/v) PEG4000 0.15 M MgCl2

220113

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