7VIJ
Crystal structure of USP7-HUBL domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U1 |
Synchrotron site | SSRF |
Beamline | BL17U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-10-25 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.97918 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 80.141, 81.429, 149.553 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 45.391 - 2.300 |
R-factor | 0.22 |
Rwork | 0.218 |
R-free | 0.26280 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2ylm |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 149.550 | 2.380 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmeas | 0.051 | 1.027 |
Number of reflections | 44009 | 4284 |
<I/σ(I)> | 22 | 2.5 |
Completeness [%] | 99.4 | |
Redundancy | 8.9 | |
CC(1/2) | 0.999 | 0.842 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | 2% v/v Tacsimate pH 7.0, 0.1M imidazole pH 7.0, 8% w/v polyethylene glycol 3350, 5% v/v 2-propanol |