5YRQ
Crystal structure of Rad5 and Rev1
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 | 2014-10-20 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97911 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 58.589, 49.280, 103.074 |
Unit cell angles | 90.00, 92.20, 90.00 |
Refinement procedure
Resolution | 29.133 - 1.999 |
R-factor | 0.2071 |
Rwork | 0.205 |
R-free | 0.24630 |
Structure solution method | SIRAS |
RMSD bond length | 0.006 |
RMSD bond angle | 0.815 |
Data reduction software | HKL-2000 (v705a) |
Data scaling software | HKL-2000 (v705a) |
Phasing software | PHASER (v7.0) |
Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.070 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.184 | 0.184 |
Number of reflections | 38367 | |
<I/σ(I)> | 16 | 6.2 |
Completeness [%] | 95.7 | 89.4 |
Redundancy | 3 | 2.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 291.15 | 18-20% PEG 3350, 100mM potassium citrate, 100mM HEPES, 5mM DTT, pH 7.0 |