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8TXM

Crystal structure of 05.GC.w13.02 Fab in complex with H1 HA from A/California/04/2009(H1N1)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 23-ID-D
Synchrotron siteAPS
Beamline23-ID-D
Temperature [K]100
Detector technologyPIXEL
Collection date2022-09-23
DetectorDECTRIS PILATUS 6M
Wavelength(s)0.97934
Spacegroup nameP 21 3
Unit cell lengths167.531, 167.531, 167.531
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution44.770 - 3.250
R-factor0.2759
Rwork0.275
R-free0.28700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4m4y
RMSD bond length0.002
RMSD bond angle0.441
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX ((1.19.2_4158: ???))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]44.7703.310
High resolution limit [Å]3.2503.250
Rpim0.053
Number of reflections249171320
<I/σ(I)>12
Completeness [%]100.0100
Redundancy13.6
CC(1/2)1.0000.670
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP2930.2 M sodium acetate, pH 6.2, 20% PEG3350

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