6P0O
Crystal structure of GDP-bound human RalA
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 4.2.2 |
Synchrotron site | ALS |
Beamline | 4.2.2 |
Temperature [K] | 100 |
Detector technology | CMOS |
Collection date | 2019-02-28 |
Detector | RDI CMOS_8M |
Wavelength(s) | 1.00003 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 64.962, 104.880, 55.549 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 39.165 - 1.540 |
R-factor | 0.1385 |
Rwork | 0.137 |
R-free | 0.17500 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1u8z |
RMSD bond length | 0.008 |
RMSD bond angle | 1.083 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((1.14_3260: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 39.170 | 1.600 |
High resolution limit [Å] | 1.540 | 1.540 |
Rmeas | 0.122 | 0.816 |
Rpim | 0.047 | 0.393 |
Number of reflections | 28327 | 2508 |
<I/σ(I)> | 12.9 | 1.6 |
Completeness [%] | 99.5 | 93.9 |
Redundancy | 6.6 | 4.1 |
CC(1/2) | 0.998 | 0.643 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 293 | 0.2 M Calcium Acetate pH 5.5 18-22% PEG3350 |