6GY4
Crystal structure of the N-terminal KH domain of human BICC1
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I04-1 |
| Synchrotron site | Diamond |
| Beamline | I04-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-09-30 |
| Detector | DECTRIS PILATUS3 6M |
| Wavelength(s) | 0.9212 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 44.406, 153.164, 86.235 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 19.740 - 1.986 |
| R-factor | 0.2579 |
| Rwork | 0.256 |
| R-free | 0.30350 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1zzk |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.514 |
| Data reduction software | XDS |
| Data scaling software | STARANISO |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.13_2998: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 19.740 | 2.164 |
| High resolution limit [Å] | 1.986 | 1.986 |
| Rmerge | 0.099 | 0.949 |
| Rpim | 0.043 | 0.457 |
| Number of reflections | 11724 | 576 |
| <I/σ(I)> | 10 | 1.6 |
| Completeness [%] | 90.5 | 67.5 |
| Redundancy | 6.4 | 5.2 |
| CC(1/2) | 0.999 | 0.682 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 277 | 0.1 M Lithium Sulfate, 50 % PEG 400, 0.1 M acetate pH 4.0 |






