6UNR
Kinase domain of ALK2-K492A/K493A with AMPPNP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.3.1 |
Synchrotron site | ALS |
Beamline | 8.3.1 |
Temperature [K] | 80 |
Detector technology | PIXEL |
Collection date | 2018-06-27 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.1111 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 59.122, 87.124, 138.916 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.140 - 2.200 |
R-factor | 0.2461 |
Rwork | 0.243 |
R-free | 0.30250 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3q4u |
RMSD bond length | 0.003 |
RMSD bond angle | 0.743 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.920 | 2.270 |
High resolution limit [Å] | 2.200 | 2.200 |
Rmerge | 0.102 | 1.172 |
Rmeas | 0.119 | 1.361 |
Rpim | 0.060 | 0.685 |
Number of reflections | 18605 | 1571 |
<I/σ(I)> | 10.6 | 1.9 |
Completeness [%] | 99.9 | |
Redundancy | 7.2 | |
CC(1/2) | 0.990 | 0.929 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 298 | 0.05 M PIPES 7 pH, 0.01 M DTT, 10 %w/v PEG 4000 |