5MPV
Crystal structure of a Mycobacterium tuberculosis chorismate mutase optimized for high autonomous activity by directed evolution
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM14 |
Synchrotron site | ESRF |
Beamline | BM14 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-04-01 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.953723 |
Spacegroup name | P 64 |
Unit cell lengths | 54.587, 54.587, 63.217 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 47.270 - 1.490 |
R-factor | 0.1911 |
Rwork | 0.190 |
R-free | 0.21875 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2w1a |
RMSD bond length | 0.020 |
RMSD bond angle | 1.892 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0151) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.270 | 1.496 |
High resolution limit [Å] | 1.488 | 1.488 |
Rmeas | 0.056 | 2.806 |
Number of reflections | 16797 | |
<I/σ(I)> | 15.01 | 0.33 |
Completeness [%] | 95.5 | 82.9 |
Redundancy | 6.2 | 2.2 |
CC(1/2) | 0.999 | 0.332 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 293 | 25% PEG MME 2000, 0.2 M trimehylamino-N-oxide, 0.1 M Tris. Microseeding. |