5WWG
Crystal structure of hnRNPA2B1 in complex with AAGGACUUGC
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-10-13 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.97776 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 132.810, 46.228, 33.994 |
Unit cell angles | 90.00, 102.22, 90.00 |
Refinement procedure
Resolution | 30.000 - 2.030 |
R-factor | 0.20145 |
Rwork | 0.199 |
R-free | 0.25628 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5en1 |
RMSD bond length | 0.016 |
RMSD bond angle | 1.831 |
Data reduction software | DENZO |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0135) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.082 |
High resolution limit [Å] | 2.030 | 2.030 |
Number of reflections | 14087 | |
<I/σ(I)> | 2.4 | |
Completeness [%] | 95.9 | |
Redundancy | 4.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 9 | 293 | 25% (w/v) PEG 1500, 0.1M MMT/Sodium hydroxide pH 9.0 |