3BPX
Crystal Structure of MarR
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 40.109, 51.527, 139.243 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 26.290 - 1.950 |
R-factor | 0.222 |
Rwork | 0.222 |
R-free | 0.28400 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3bpv |
RMSD bond length | 0.006 |
RMSD bond angle | 1.000 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | AMoRE |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 30.000 |
High resolution limit [Å] | 1.950 |
Number of reflections | 19316 |
<I/σ(I)> | 15 |
Completeness [%] | 91.2 |
Redundancy | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5 | 296 | 12% PEG 3350 8% isopropanol 0.1M NaK tartrate 0.1M Na citrate, pH 5.0, VAPOR DIFFUSION, HANGING DROP, temperature 296K |