5AC8
S. enterica HisA with mutations D10G, dup13-15, G102A
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2013-07-25 |
Detector | DECTRIS PILATUS 6M |
Spacegroup name | P 61 2 2 |
Unit cell lengths | 86.415, 86.415, 122.027 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 47.289 - 1.699 |
R-factor | 0.1969 |
Rwork | 0.196 |
R-free | 0.20920 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5ahf |
RMSD bond length | 0.008 |
RMSD bond angle | 1.152 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.800 |
High resolution limit [Å] | 1.700 | 1.700 |
Rmerge | 0.140 | 1.390 |
Number of reflections | 30311 | |
<I/σ(I)> | 14.96 | 1.67 |
Completeness [%] | 99.8 | 99 |
Redundancy | 19 | 17.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 4.6 | 2.0M AMMONIUM SULFATE, 0.1M SODIUM ACETATE PH4.6 |