5GK9
Crystal structure of human HBO1 in complex with BRPF2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-10-31 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9786 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 126.470, 39.321, 87.666 |
Unit cell angles | 90.00, 122.10, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.400 |
R-factor | 0.26 |
Rwork | 0.233 |
R-free | 0.26000 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2giv |
RMSD bond length | 0.015 |
RMSD bond angle | 1.777 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.490 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.078 | 0.522 |
Number of reflections | 14322 | |
<I/σ(I)> | 18 | 3.6 |
Completeness [%] | 97.9 | 97.9 |
Redundancy | 3.7 | 3.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | Tacsimate Tris-HCl, PEG 3350 |