2XS6
CRYSTAL STRUCTURE OF THE RHOGAP DOMAIN OF HUMAN PIK3R2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.2 |
Synchrotron site | BESSY |
Beamline | 14.2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-03-17 |
Detector | MARRESEARCH |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 94.661, 34.354, 71.317 |
Unit cell angles | 90.00, 130.88, 90.00 |
Refinement procedure
Resolution | 53.920 - 2.090 |
R-factor | 0.1942 |
Rwork | 0.191 |
R-free | 0.23980 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1pbw |
RMSD bond length | 0.007 |
RMSD bond angle | 1.032 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0102) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.330 | 2.210 |
High resolution limit [Å] | 2.090 | 2.090 |
Rmerge | 0.050 | 0.210 |
Number of reflections | 9968 | |
<I/σ(I)> | 9.9 | 3.7 |
Completeness [%] | 95.6 | 76.6 |
Redundancy | 3.7 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6.5 | PROTEIN WAS CRYSTALLIZED FROM 0.1 M NACL, 0.85 M TRI-SODIUM CITRATE DIHYDRATE AND 0.1 M SODIUM CACODYLATE PH 6.5. |