2XET
Conserved hydrophobic clusters on the surface of the Caf1A usher C-terminal domain are important for F1 antigen assembly
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 | 2008-06-28 |
| Detector | ADSC CCD |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 39.669, 40.336, 44.862 |
| Unit cell angles | 90.00, 92.69, 90.00 |
Refinement procedure
| Resolution | 40.000 - 1.600 |
| R-factor | 0.1678 |
| Rwork | 0.167 |
| R-free | 0.20900 |
| Structure solution method | SIRAS |
| Starting model (for MR) | NONE |
| RMSD bond length | 0.012 |
| RMSD bond angle | 1.333 |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | SHELX |
| Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 40.000 | 1.640 |
| High resolution limit [Å] | 1.600 | 1.600 |
| Rmerge | 0.080 | 0.390 |
| Number of reflections | 17753 | |
| <I/σ(I)> | 12.3 | 3.5 |
| Completeness [%] | 94.3 | 80.2 |
| Redundancy | 3.7 | 3.5 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | 3 | 0.2M LISO4, 12-15% PEG8000, 4% PEG400, 0.1M NA-CITRATE PH2.8-3.0, PROTEIN 15 G/L, MIXED 1:1, MICROSEEDING | ||
| 1 | 3 | 0.2M LISO4, 12-15% PEG8000, 4% PEG400, 0.1M NA-CITRATE PH2.8-3.0, PROTEIN 15 G/L, MIXED 1:1, MICROSEEDING |






