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 |