4JQF
Structure of the C-terminal domain of human telomeric Stn1
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X25 |
Synchrotron site | NSLS |
Beamline | X25 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2011-12-05 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 1.0076, 1.1000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 28.805, 76.572, 114.422 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 20.000 - 1.600 |
R-factor | 0.19852 |
Rwork | 0.197 |
R-free | 0.21899 |
Structure solution method | MAD |
RMSD bond length | 0.007 |
RMSD bond angle | 0.938 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SOLVE |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 1.641 |
High resolution limit [Å] | 1.600 | 1.600 |
Rmerge | 0.059 | 0.486 |
Number of reflections | 34343 | |
<I/σ(I)> | 13.8 | 2.3 |
Completeness [%] | 99.9 | 99.8 |
Redundancy | 5.6 | 4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 8.5 | 289.15 | 1.6 M Ammonium phosphate dibasic, 100 mM Tris, 3% Ethylene glycol, pH 8.5, VAPOR DIFFUSION, Microbatch Crystallization, temperature 289.15K |