6ZIO
CRYSTAL STRUCTURE OF NRAS (C118S) IN COMPLEX WITH GDP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-10-11 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1.0 |
Spacegroup name | P 1 |
Unit cell lengths | 37.174, 37.161, 66.245 |
Unit cell angles | 78.83, 75.24, 64.70 |
Refinement procedure
Resolution | 19.190 - 1.550 |
R-factor | 0.239 |
Rwork | 0.237 |
R-free | 0.27800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3con |
RMSD bond length | 0.008 |
RMSD bond angle | 0.950 |
Data reduction software | XDS |
Data scaling software | STARANISO |
Phasing software | PHASER |
Refinement software | BUSTER (2.11.7) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.190 | 1.684 |
High resolution limit [Å] | 1.550 | 1.555 |
Rmerge | 0.100 | 0.451 |
Number of reflections | 28360 | 1419 |
<I/σ(I)> | 7.5 | 2.1 |
Completeness [%] | 83.5 | |
Redundancy | 2.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 278 | 25% PEG 2000, 100mM HEPES PH=7.5 |