4L45
Crystal structures of human p70S6K1-T389E
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-10-07 |
Detector | CCD ADSC unsupported-q315 |
Wavelength(s) | 0.9796 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 81.191, 81.191, 110.744 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 43.540 - 2.900 |
R-factor | 0.235 |
Rwork | 0.232 |
R-free | 0.28650 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3a62 |
RMSD bond length | 0.005 |
RMSD bond angle | 1.092 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Inner shell | |
Low resolution limit [Å] | 50.000 | 50.000 |
High resolution limit [Å] | 2.900 | 6.030 |
Rmerge | 0.077 | 0.037 |
Number of reflections | 9796 | |
<I/σ(I)> | 12.8 | |
Completeness [%] | 99.9 | 99.3 |
Redundancy | 5.3 | 4.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | hanging drop | 6.5 | 289 | 1.4M sodium citrate, 0.1M sodium cacodylate, pH 6.5, hanging drop, temperature 289K |