7V58
Structural insights into the substrate selectivity of acyl-CoA transferase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSRRC BEAMLINE BL15A1 |
Synchrotron site | NSRRC |
Beamline | BL15A1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2019-11-09 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.99 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 62.724, 122.630, 136.462 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 25.540 - 1.840 |
R-factor | 0.1872 |
Rwork | 0.185 |
R-free | 0.22570 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1fc4 |
RMSD bond length | 0.012 |
RMSD bond angle | 1.144 |
Data scaling software | HKL-2000 |
Refinement software | REFMAC (1.17.1_3660) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 1.910 |
High resolution limit [Å] | 1.840 | 1.840 |
Rmerge | 0.042 | 0.729 |
Number of reflections | 90896 | 9025 |
<I/σ(I)> | 32.6 | |
Completeness [%] | 99.2 | |
Redundancy | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 295 | 0.2 M ammonium sulfate, 0.1 M MES monohydrate, pH 6.5, 0.2 M Lithium sulfate, 1 mM L-glycine, 30% polyethylene glycol (PEG) 5000 |