5JRV
Crystal structure of Fe(II) NO-bound H-NOX protein from C. subterraneus
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.2.2 |
| Synchrotron site | ALS |
| Beamline | 8.2.2 |
| Temperature [K] | 80 |
| Detector technology | CCD |
| Collection date | 2015-02-27 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.999919 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 80.385, 127.626, 42.937 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 49.979 - 1.953 |
| R-factor | 0.2031 |
| Rwork | 0.202 |
| R-free | 0.23130 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1u55 |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.780 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | MOLREP |
| Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.020 |
| High resolution limit [Å] | 1.950 | 1.950 |
| Rmerge | 0.093 | 0.434 |
| Number of reflections | 32785 | |
| <I/σ(I)> | 14.9 | 3.67 |
| Completeness [%] | 99.9 | 100 |
| Redundancy | 6.8 | |
| CC(1/2) | 0.909 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | Anaerobically grown under Argon. 20 mg/mL protein with well condition of 0.15 M NaI, 25% PEG3350. |






