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4D5T

Structure of N-terminally truncated A49 from Vaccinia Virus Western Reserve

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04-1
Synchrotron siteDiamond
BeamlineI04-1
Temperature [K]100
Detector technologyPIXEL
Collection date2013-03-02
DetectorDECTRIS PILATUS 2M
Spacegroup nameP 1 21 1
Unit cell lengths92.290, 45.630, 160.260
Unit cell angles90.00, 98.74, 90.00
Refinement procedure
Resolution45.710 - 1.840
R-factor0.20801
Rwork0.206
R-free0.23888
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)4d5r
RMSD bond length0.017
RMSD bond angle1.689
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareMOLREP
Refinement softwareREFMAC (5.8.0069)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]45.7001.890
High resolution limit [Å]1.8401.840
Rmerge0.0701.160
Number of reflections112855
<I/σ(I)>13.61.5
Completeness [%]97.996
Redundancy6.86.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1293PROTEIN (1 UL AT 25.0 MG/ML) WAS MIXED WITH 1 UL RESERVOIR SOLUTION AND EQUILIBRATED AT 20 C AGAINST 500 UL RESERVOIRS CONTAINING 0.1 M HEPES PH 7.5, 1.6 M AMMONIUM SULFATE AND 1.5% (VOL/VOL) PEG 400. CRYSTALS WERE CRYOPROTECTED BY PASSAGE THROUGH 2 UL OF PERFLUOROPOLYETHER OIL (HAMPTON RESEARCH) THAT HAD BEEN OVERLAID ONTO THE MOTHER LIQUOR.

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PDB entries from 2024-05-15

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