2ETX
Crystal Structure of MDC1 Tandem BRCT Domains
Experimental procedure
| Experimental method | MAD |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 19-ID |
| Synchrotron site | APS |
| Beamline | 19-ID |
| Temperature [K] | 100 |
| Wavelength(s) | 0.97954, 0.97967, 0.98120 |
| Spacegroup name | P 1 |
| Unit cell lengths | 41.890, 44.350, 63.100 |
| Unit cell angles | 70.98, 86.45, 61.91 |
Refinement procedure
| Resolution | 59.340 - 1.330 |
| R-factor | 0.20279 |
| Rwork | 0.202 |
| R-free | 0.22574 |
| Structure solution method | MAD |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.296 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | SOLVE |
| Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 36.840 | 1.364 |
| High resolution limit [Å] | 1.330 | 1.330 |
| Number of reflections | 85639 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 6 | 293 | MES 0.1M, PEG 8000 15%, ETHYLENE GLYCOL 15%, AMMONIUM ACETATE 0.2M, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K |






