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6HG0

Influenza A Virus N9 Neuraminidase complex with NANA (Tern/Australia).

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRL BEAMLINE BL11-1
Synchrotron siteSSRL
BeamlineBL11-1
Temperature [K]100
Detector technologyCCD
Collection date2001-12-14
DetectorADSC QUANTUM 315
Wavelength(s)0.98
Spacegroup nameI 4 3 2
Unit cell lengths181.200, 181.200, 181.200
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution48.470 - 1.300
R-factor0.0927
Rwork0.091
R-free0.11993
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)7nn9
RMSD bond length0.020
RMSD bond angle2.082
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwareREFMAC
Refinement softwareREFMAC (5.8.0230)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]48.4701.320
High resolution limit [Å]1.3001.300
Number of reflections1223856028
<I/σ(I)>16.74.3
Completeness [%]99.7100
Redundancy1410.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.6293N9 crystals were grown by hanging-drop vapour diffusion against a reservoir of 1.9M potassium phosphate, pH 6.8, starting with equal volumes of N9 NA (10-15 mg/ml in water) and potassium phosphate buffer 1.4M KH2PO4:3M K2HPO4 in ratio 8:4, pH 6.6 at 20 degrees celsius. Inhibitor complexes obtained by soaking N9 crystals in a solution of 1.4M potassium phosphate buffer, pH 6.8, containing 5mM of inhibitor for 3 hours at 4 degrees celsius. Soaked in glycerol cryo-buffer.

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