2GJT
Crystal structure of the human receptor phosphatase PTPRO
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 | 2005-03-24 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.95 |
Spacegroup name | P 65 |
Unit cell lengths | 131.060, 131.060, 77.530 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 42.910 - 2.150 |
R-factor | 0.18192 |
Rwork | 0.179 |
R-free | 0.23366 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2ahs |
RMSD bond length | 0.017 |
RMSD bond angle | 1.587 |
Data reduction software | MOSFLM |
Data scaling software | CCP4 ((SCALA)) |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.910 | 2.250 |
High resolution limit [Å] | 2.150 | 2.150 |
Number of reflections | 41322 | |
Completeness [%] | 99.9 | 99.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 277 | Isopropanol, PEG4K, pH 8, VAPOR DIFFUSION, SITTING DROP, temperature 277K |