2OVE
Crystal Structure of Recombinant Human Complement Protein C8gamma
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-BM |
Synchrotron site | APS |
Beamline | 19-BM |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2003-02-16 |
Detector | ADSC QUANTUM 210 |
Wavelength(s) | 0.98925 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 42.227, 59.775, 71.901 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 500.000 - 2.000 |
Rwork | 0.226 |
R-free | 0.26000 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.006 |
RMSD bond angle | 1.148 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | CNS |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.070 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.046 | 0.114 |
Number of reflections | 12610 | |
<I/σ(I)> | 12.6 | 8.5 |
Completeness [%] | 97.8 | 95 |
Redundancy | 4.3 | 4.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4 | 290 | 0.1 M sodium citrate and 25-27% PEG 4000, pH 4.0, VAPOR DIFFUSION, HANGING DROP, temperature 290K |