5NVN
Crystal structure of the human 4EHP-4E-BP1 complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-10-21 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 0.99999 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 38.400, 83.390, 70.500 |
Unit cell angles | 90.00, 104.28, 90.00 |
Refinement procedure
Resolution | 41.695 - 1.900 |
R-factor | 0.2277 |
Rwork | 0.226 |
R-free | 0.25060 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2jgb |
RMSD bond length | 0.003 |
RMSD bond angle | 0.529 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.700 | 1.950 |
High resolution limit [Å] | 1.900 | 1.900 |
Number of reflections | 33907 | |
<I/σ(I)> | 8.5 | 2.07 |
Completeness [%] | 99.7 | 99.6 |
Redundancy | 6.6 | 6.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 0.1 M sodium acetate pH 4.6 1.7 M sodium formate |