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7KMJ

Hsa Siglec and Unique domains in complex with Sialyl Lewis C

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL9-2
Synchrotron siteSSRL
BeamlineBL9-2
Temperature [K]100
Detector technologyPIXEL
Collection date2019-11-21
DetectorDECTRIS PILATUS3 S 6M
Wavelength(s)0.9795
Spacegroup nameP 21 21 21
Unit cell lengths46.635, 58.173, 75.973
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution37.990 - 1.330
R-factor0.1924
Rwork0.191
R-free0.21600
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5eq2
RMSD bond length0.012
RMSD bond angle1.510
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]50.0001.320
High resolution limit [Å]1.3001.300
Number of reflections17487092468
<I/σ(I)>40.5
Completeness [%]99.7
Redundancy8
CC(1/2)0.9980.891
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP29821.6 mg/ml in 20 mM Tris-HCl, pH 7.2. Equilibrate 1 ul protein and 2 ul reservoir solution over 50 ul of reservoir solution (0.1 M Succinate/Phosphate/Glycine pH 10.0 and 25% PEG 3350). Crystals were soaked in reservoir solution supplemented with 5 mM of sLec for 20 hr

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