2C2H
CRYSTAL STRUCTURE OF THE HUMAN RAC3 IN COMPLEX WITH GDP
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 | 2005-09-03 |
Detector | MARRESEARCH |
Spacegroup name | H 3 |
Unit cell lengths | 110.320, 110.320, 81.790 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 62.140 - 1.850 |
R-factor | 0.195 |
Rwork | 0.194 |
R-free | 0.22900 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1g4u |
RMSD bond length | 0.012 |
RMSD bond angle | 1.773 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 27.070 | 1.900 |
High resolution limit [Å] | 1.850 | 1.800 |
Rmerge | 0.070 | 0.510 |
Number of reflections | 28734 | |
<I/σ(I)> | 10.99 | 2 |
Completeness [%] | 91.3 | 93.1 |
Redundancy | 3.24 | 2.76 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | 30% MPD, 0.5 M AMMONIUM SULFATE, 0.1 M HEPES PH 4.5 |