3OZI
Crystal structure of the TIR domain from the flax disease resistance protein L6
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Detector technology | CCD |
| Collection date | 2009-09-20 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.953693 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 65.941, 102.241, 58.300 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 19.296 - 2.300 |
| R-factor | 0.1766 |
| Rwork | 0.174 |
| R-free | 0.22970 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3jrn |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.001 |
| Data scaling software | SCALA (3.3.9) |
| Phasing software | PHASER (2.1.4) |
| Refinement software | PHENIX (1.6.4_486) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 55.415 | 19.531 | 2.420 |
| High resolution limit [Å] | 2.300 | 7.270 | 2.300 |
| Rmerge | 0.033 | 0.321 | |
| Rmeas | 0.036 | 0.347 | |
| Rpim | 0.014 | 0.129 | |
| Total number of observations | 3978 | 18309 | |
| Number of reflections | 18088 | ||
| <I/σ(I)> | 16.7 | 32.5 | 6.7 |
| Completeness [%] | 99.7 | 94.9 | 99.8 |
| Redundancy | 7.2 | 6.5 | 7 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 5.2 | 293 | 36% PEG 200, 0.1M sodium acetate, pH 5.2, 10mM hexammine cobalt(III) chloride, VAPOR DIFFUSION, HANGING DROP, temperature 293K |






