2WH5
Crystal structure of human acyl-CoA binding domain 4 complexed with stearoyl-CoA
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-03-27 |
Detector | MARRESEARCH |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 85.060, 95.100, 119.740 |
Unit cell angles | 90.00, 110.28, 90.00 |
Refinement procedure
Resolution | 42.528 - 2.600 |
R-factor | 0.2069 |
Rwork | 0.206 |
R-free | 0.23650 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1hbk |
RMSD bond length | 0.010 |
RMSD bond angle | 1.481 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 79.780 | 2.600 |
High resolution limit [Å] | 2.550 | 2.550 |
Rmerge | 0.080 | 0.480 |
Number of reflections | 58524 | |
<I/σ(I)> | 4.5 | 2 |
Completeness [%] | 95.0 | 91 |
Redundancy | 4 | 3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 0.24M K_THIOCYANATE; 26W/V PEG_3350 |