4ASI
Crystal structure of human ACACA C-terminal domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I02 |
Synchrotron site | Diamond |
Beamline | I02 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-10-05 |
Detector | ADSC CCD |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 109.966, 143.712, 540.072 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 540.070 - 2.800 |
R-factor | 0.20367 |
Rwork | 0.202 |
R-free | 0.23589 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ENTRIES 2X24 AND 3FF6 |
RMSD bond length | 0.011 |
RMSD bond angle | 1.432 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 143.710 | 2.950 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.170 | |
Number of reflections | 207126 | |
<I/σ(I)> | 8 | 0.8 |
Completeness [%] | 98.4 | 98.2 |
Redundancy | 4.1 | 4.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 0.05M NA MALONATE; 19% (W/V) PEG3350 |