6Y24
Crystal structure of fourth KH domain of FUBP1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.2 |
Synchrotron site | BESSY |
Beamline | 14.2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-03-28 |
Detector | DECTRIS PILATUS3 2M |
Wavelength(s) | 0.9184 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 69.996, 89.054, 28.711 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 35.020 - 1.860 |
R-factor | 0.1961 |
Rwork | 0.194 |
R-free | 0.24280 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4lij |
RMSD bond length | 0.016 |
RMSD bond angle | 1.546 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 55.040 | 1.900 |
High resolution limit [Å] | 1.860 | 1.860 |
Number of reflections | 7912 | 486 |
<I/σ(I)> | 9.4 | |
Completeness [%] | 100.0 | |
Redundancy | 6.1 | |
CC(1/2) | 0.996 | 0.779 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 3.1 M sodium formate |