3UOT
Crystal Structure of MDC1 FHA Domain in Complex with a Phosphorylated Peptide from the MDC1 N-terminus
Experimental procedure
Experimental method | SAD |
Source type | SYNCHROTRON |
Source details | SRS BEAMLINE PX10.1 |
Synchrotron site | SRS |
Beamline | PX10.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-05-23 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.961 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 58.485, 59.880, 72.081 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 15.000 - 1.800 |
R-factor | 0.20687 |
Rwork | 0.205 |
R-free | 0.24262 |
Structure solution method | SAD |
RMSD bond length | 0.010 |
RMSD bond angle | 1.481 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | SOLVE |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.000 | 1.860 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.037 | 0.315 |
Number of reflections | 24225 | |
Completeness [%] | 93.4 | 55.3 |
Redundancy | 3.2 | 2.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | MICROBATCH | 5.5 | 291 | 25% v/v ethanol, 0.1M sodium acetate pH 5.5, Microbatch, temperature 291K |