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2VFP

Low Temperature Structure of P22 Tailspike Protein Fragment (109-666), Mutant V349L

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.1
Synchrotron siteBESSY
Beamline14.1
Temperature [K]100
Detector technologyCCD
Collection date2006-10-29
DetectorMARRESEARCH
Spacegroup nameP 21 3
Unit cell lengths120.290, 120.290, 120.290
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution49.090 - 1.550
R-factor0.125
Rwork0.123
R-free0.15200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2vfo
RMSD bond length0.011
RMSD bond angle1.376
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwareREFMAC (5.2.0005)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.700
High resolution limit [Å]1.5901.590
Rmerge0.0600.210
Number of reflections72574
<I/σ(I)>26.14
Completeness [%]93.355.8
Redundancy10.51.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
110DROP: 2 MICROLITER 1.5 M AMMONIUM SULFATE, 0.1 M SODIUM PHOSPHATE, PH 10.0, PLUS 3.3 MICROLITER 10 MG/ML PROTEIN SOLUTION IN 10 MM HEPES, PH 7.0; RESERVOIR: 750 MICOLITER 1.0 M AMMONIUM SULFATE, 0.1 M SODIUM PHOSPHATE, PH 10.0

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