2XGD
Crystal structure of a designed homodimeric variant T-A(L)A(L) of the tetracycline repressor
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | BESSY BEAMLINE 14.1 |
| Synchrotron site | BESSY |
| Beamline | 14.1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Detector | RAYONIX |
| Spacegroup name | I 41 2 2 |
| Unit cell lengths | 69.656, 69.656, 184.328 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 34.840 - 2.250 |
| R-factor | 0.22032 |
| Rwork | 0.217 |
| R-free | 0.25886 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1a6i |
| RMSD bond length | 0.014 |
| RMSD bond angle | 1.445 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 40.000 | 2.390 |
| High resolution limit [Å] | 2.250 | 2.250 |
| Rmerge | 0.060 | 0.690 |
| Number of reflections | 11142 | |
| <I/σ(I)> | 28.2 | 4.2 |
| Completeness [%] | 99.3 | 96.2 |
| Redundancy | 19.4 | 14.1 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 |






