2UWI
Structure of CrmE, a poxvirus TNF receptor
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-05-14 |
Detector | ADSC CCD |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 41.380, 56.490, 122.530 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 39.193 - 2.000 |
Rwork | 0.210 |
R-free | 0.24650 |
Structure solution method | MAD |
Starting model (for MR) | NONE |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | autoSHARP |
Refinement software | BUSTER (TNT) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 100.000 | 2.070 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.110 | 0.880 |
Number of reflections | 20089 | |
<I/σ(I)> | 11.1 | 1.4 |
Completeness [%] | 99.9 | 100 |
Redundancy | 3.5 | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5 | 293 | 100 NL PROTEIN (6 MG/ML CRME IN 20 MM TRIS 150 MM NACL PH 8.0) AND 100 NL RESERVOIR (0.1 M CITRATE PH 5.0 PLUS 30% W/V PEG 6000) SITTING DROPS AT 20C EQUILIBRATED AGAINST 100 UL RESERVOIRS. |