3KFO
Crystal structure of the C-terminal domain from the nuclear pore complex component NUP133 from Saccharomyces cerevisiae
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 31-ID |
Synchrotron site | APS |
Beamline | 31-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-07-31 |
Detector | RAYONIX MX225HE |
Wavelength(s) | 0.97929 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 47.433, 52.678, 76.674 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 23.000 - 1.900 |
R-factor | 0.193 |
Rwork | 0.191 |
R-free | 0.24500 |
Structure solution method | SAD |
RMSD bond length | 0.018 |
RMSD bond angle | 1.635 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SHELX (C) |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 31.000 | 2.000 |
High resolution limit [Å] | 1.900 | 1.900 |
Number of reflections | 15683 | |
<I/σ(I)> | 10.6 | 4.6 |
Completeness [%] | 99.7 | 100 |
Redundancy | 7.7 | 7.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 294 | 20% PEG 3350, 200mM Potassium Thiocyanate, VAPOR DIFFUSION, SITTING DROP, temperature 294K |