6A8W
Crystal structure of the FHA domain of Far9
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL17U1 |
| Synchrotron site | SSRF |
| Beamline | BL17U1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2015-10-11 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.9792 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 31.991, 59.414, 64.984 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 29.707 - 1.844 |
| R-factor | 0.1937 |
| Rwork | 0.191 |
| R-free | 0.22270 |
| Structure solution method | SAD |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.875 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHENIX |
| Refinement software | PHENIX ((1.12_2829: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 1.880 |
| High resolution limit [Å] | 1.850 | 1.850 |
| Rmerge | 0.186 | |
| Rmeas | 0.193 | |
| Rpim | 0.053 | 0.403 |
| Number of reflections | 11148 | 550 |
| <I/σ(I)> | 19.6 | 2.4 |
| Completeness [%] | 99.6 | 98.7 |
| Redundancy | 13.2 | 11.1 |
| CC(1/2) | 0.759 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 289 | 6%(v/v) Tacsimate pH 6.0; 0.1M MES pH 6.0; 25%(w/v) polyethylene glycol 4,000. |






