8E0A
Crystal structure of human Sar1b
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CHESS BEAMLINE A1 |
Synchrotron site | CHESS |
Beamline | A1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-12-05 |
Detector | ADSC QUANTUM 210 |
Wavelength(s) | 0.9778 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 52.966, 61.485, 70.589 |
Unit cell angles | 90.00, 107.34, 90.00 |
Refinement procedure
Resolution | 29.545 - 1.797 |
R-factor | 0.171 |
Rwork | 0.169 |
R-free | 0.20880 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 8dzm |
RMSD bond length | 0.006 |
RMSD bond angle | 1.042 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.830 |
High resolution limit [Å] | 1.790 | 1.790 |
Rmerge | 0.073 | 0.303 |
Number of reflections | 40321 | 2011 |
<I/σ(I)> | 32.5 | 5 |
Completeness [%] | 99.8 | 100 |
Redundancy | 3.8 | 3.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 1.2M (NH4)2SO4 and 0.1M sodium citrate, pH5.5. |