7D0O
Crystal structure of human HBO1-BRPF2 in apo form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-04-16 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 0.97892 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 127.604, 38.372, 88.075 |
Unit cell angles | 90.00, 122.60, 90.00 |
Refinement procedure
Resolution | 50.010 - 2.510 |
R-factor | 0.2478 |
Rwork | 0.246 |
R-free | 0.29010 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5gk9 |
RMSD bond length | 0.007 |
RMSD bond angle | 1.243 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHENIX |
Refinement software | REFMAC (5.8.0155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.010 | 2.590 |
High resolution limit [Å] | 2.500 | 2.500 |
Number of reflections | 11980 | 912 |
<I/σ(I)> | 25.9 | 2.2 |
Completeness [%] | 95.0 | 73.8 |
Redundancy | 6.1 | 4.8 |
CC(1/2) | 0.970 | 0.980 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | Tacsimate Tris-HCl, PEG 3350 |