5K5X
Crystal structure of human PDGFRA
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-01-10 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9785 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 101.599, 101.599, 110.665 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 40.882 - 2.168 |
R-factor | 0.1931 |
Rwork | 0.192 |
R-free | 0.22370 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1rjb |
RMSD bond length | 0.008 |
RMSD bond angle | 1.036 |
Data reduction software | DENZO |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.4_1496) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.250 |
High resolution limit [Å] | 2.168 | 2.170 |
Rmerge | 0.036 | |
Number of reflections | 35322 | |
<I/σ(I)> | 20.95 | 2.05 |
Completeness [%] | 100.0 | 100 |
Redundancy | 16.6 | 14.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.1M HEPES pH7.5, 1.6M (NH4)2SO4, 0.1M NaCl |