3KV7
Structural basis of the activity and substrate specificity of the fluoroacetyl-CoA thioesterase FlK - wild type FlK in complex with acetate
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-4 |
Synchrotron site | ESRF |
Beamline | ID14-4 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9795 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 62.300, 92.720, 49.270 |
Unit cell angles | 90.00, 100.89, 90.00 |
Refinement procedure
Resolution | 23.900 - 1.560 |
R-factor | 0.17441 |
Rwork | 0.173 |
R-free | 0.20481 |
Starting model (for MR) | 1hnn |
RMSD bond length | 0.031 |
RMSD bond angle | 2.335 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | AMoRE |
Refinement software | REFMAC (5.5.0102) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.530 | 1.650 |
High resolution limit [Å] | 1.560 | 1.560 |
Number of reflections | 38789 | |
Completeness [%] | 99.7 | 99 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 298 | Tris HCl Peg4000 Sodium acetate, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K |