4I1K
Crystal Structure of VRN1 (Residues 208-341)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-08-16 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.956 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 106.152, 47.310, 61.413 |
Unit cell angles | 90.00, 114.97, 90.00 |
Refinement procedure
Resolution | 50.000 - 1.600 |
Rwork | 0.120 |
R-free | 0.16600 |
Structure solution method | SAD |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | AutoSol |
Refinement software | PHENIX ((phenix.refine: dev_1031)) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 1.600 |
Number of reflections | 34680 |
Completeness [%] | 100.0 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6 | 277 | 19 mg/mL protein in 10 mM HEPES, pH 7.0, 50 mM sodium chloride, 5 mM DTT + equal volume well solution (0.1 M MES, pH 6.0, 1.4 M sodium chloride, 10 mM manganese chloride), VAPOR DIFFUSION, HANGING DROP, temperature 277K |