5IXR
Crystal Structure of C139A nostoc H-NOX domain with imidazole
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL9-2 |
Synchrotron site | SSRL |
Beamline | BL9-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-02-02 |
Detector | MARMOSAIC 325 mm CCD |
Wavelength(s) | 0.97945 |
Spacegroup name | P 21 3 |
Unit cell lengths | 123.051, 123.051, 123.051 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 43.510 - 2.500 |
R-factor | 0.13282 |
Rwork | 0.131 |
R-free | 0.17353 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4iam |
RMSD bond length | 0.013 |
RMSD bond angle | 1.718 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0073) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 43.510 | 2.590 |
High resolution limit [Å] | 2.500 | 2.500 |
Number of reflections | 20550 | |
<I/σ(I)> | 24.2 | 2.3 |
Completeness [%] | 99.5 | 100 |
Redundancy | 6.2 | 6.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 295 | 1.9M sodium malonate, pH 7.0, |