3VK6
Crystal structure of a phosphotyrosine binding domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X4A |
Synchrotron site | NSLS |
Beamline | X4A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-07-20 |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 0.979 |
Spacegroup name | P 62 2 2 |
Unit cell lengths | 64.657, 64.657, 121.035 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 25.228 - 1.900 |
R-factor | 0.2216 |
Rwork | 0.219 |
R-free | 0.24240 |
Structure solution method | SAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.172 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | SOLVE |
Refinement software | PHENIX ((phenix.refine: 1.6_289)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.970 |
High resolution limit [Å] | 1.900 | 1.900 |
Number of reflections | 21480 | |
<I/σ(I)> | 21.3 | |
Completeness [%] | 99.7 | 99.7 |
Redundancy | 22.8 | 22.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 289 | 200mM Li2SO4, 100mM Tris, 20% PEG 5000 MME, pH 8, VAPOR DIFFUSION, HANGING DROP, temperature 289K |