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2VFM

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

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.1
Synchrotron siteBESSY
Beamline14.1
Temperature [K]100
Detector technologyCCD
Collection date2007-05-02
DetectorMARRESEARCH
Spacegroup nameP 21 3
Unit cell lengths119.900, 119.900, 119.900
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution39.970 - 1.500
R-factor0.136
Rwork0.135
R-free0.16400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2vfq
RMSD bond length0.010
RMSD bond angle1.330
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.700
High resolution limit [Å]1.5901.590
Rmerge0.0400.150
Number of reflections74828
<I/σ(I)>37.97.2
Completeness [%]97.186.8
Redundancy10.63.1
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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