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8QWS

Crystal structure of CotB2 variant V80L in complex with alendronate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPETRA III, EMBL c/o DESY BEAMLINE P14 (MX2)
Synchrotron sitePETRA III, EMBL c/o DESY
BeamlineP14 (MX2)
Temperature [K]100
Detector technologyPIXEL
Collection date2021-03-26
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.9766
Spacegroup nameP 21 21 21
Unit cell lengths61.173, 98.514, 107.417
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution47.160 - 1.600
R-factor0.1734
Rwork0.172
R-free0.20520
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)6ggj
RMSD bond length0.012
RMSD bond angle1.127
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.700
High resolution limit [Å]1.6001.600
Rmerge2.540
Rmeas0.099
Number of reflections8612313768
<I/σ(I)>16.51.5
Completeness [%]99.999.8
Redundancy13.413.1
CC(1/2)0.9900.990
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP2917 % PEG8000, 0.15 M Mgacetate, 10% ethylenglycol

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