2IVX
Crystal structure of human cyclin T2 at 1.8 A resolution
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-03-24 |
Detector | MARRESEARCH |
Spacegroup name | P 1 |
Unit cell lengths | 43.032, 58.636, 65.634 |
Unit cell angles | 110.63, 102.41, 90.12 |
Refinement procedure
Resolution | 59.760 - 1.800 |
R-factor | 0.192 |
Rwork | 0.191 |
R-free | 0.22300 |
Structure solution method | SAD |
RMSD bond length | 0.011 |
RMSD bond angle | 1.131 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | SHELXCD |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.860 | 1.900 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.110 | 0.320 |
Number of reflections | 53530 | |
<I/σ(I)> | 14.31 | 5.36 |
Completeness [%] | 99.0 | 94.4 |
Redundancy | 3.57 | 2.67 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 0.2M NA-FORMATE, 0.1M BIS-TRIS-PROPANE PH 8.5, 20%PEG3350, 10% ETHYLENE GLYCOL, 150 NL SITTING DROP |