1TV2
Crystal structure of the hydroxylamine MtmB complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL9-1 |
Synchrotron site | SSRL |
Beamline | BL9-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2002-05-11 |
Detector | MARRESEARCH |
Wavelength(s) | 0.99200 |
Spacegroup name | P 63 2 2 |
Unit cell lengths | 158.170, 158.170, 136.210 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.970 - 2.000 |
R-factor | 0.165 |
Rwork | 0.165 |
R-free | 0.18300 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 1nth |
RMSD bond length | 0.005 |
RMSD bond angle | 1.200 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | CNS |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 2.030 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.177 | 0.593 |
Number of reflections | 67189 | |
<I/σ(I)> | 11.1 | 2.2 |
Completeness [%] | 98.9 | 99.6 |
Redundancy | 6.9 | 6.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 277 | NACL, HEPES, pH 7.50, VAPOR DIFFUSION, HANGING DROP, temperature 277K |