2B5N
Crystal Structure of the DDB1 BPB Domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 5.0.2 |
Synchrotron site | ALS |
Beamline | 5.0.2 |
Temperature [K] | 173 |
Detector technology | CCD |
Collection date | 2004-03-06 |
Wavelength(s) | 1.0 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 101.543, 73.747, 136.778 |
Unit cell angles | 90.00, 111.73, 90.00 |
Refinement procedure
Resolution | 48.800 - 2.800 |
R-factor | 0.2421 |
Rwork | 0.236 |
R-free | 0.29590 |
Structure solution method | MOLECULAR REPLACEMENT |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | AMoRE |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 48.800 |
High resolution limit [Å] | 2.540 |
Number of reflections | 62244 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 277 | PEG 4000, iso-propanol, HEPES, DTT, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K |