7E1T
Crystal structure of Rab9A-GTP-Nde1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-11-07 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.9785 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 67.421, 67.646, 118.516 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 47.750 - 2.450 |
R-factor | 0.1962 |
Rwork | 0.194 |
R-free | 0.24380 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4qxa |
RMSD bond length | 0.008 |
RMSD bond angle | 1.202 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | REFMAC (5.8.0123) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.750 | 2.510 |
High resolution limit [Å] | 2.450 | 2.450 |
Rmerge | 0.170 | |
Number of reflections | 18238 | 912 |
<I/σ(I)> | 8.5 | 2 |
Completeness [%] | 88.5 | 65.2 |
Redundancy | 5.4 | |
CC(1/2) | 0.991 | 0.715 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 5.5 | 290 | 0.1 M Bis-Tris, pH 5.5 and 25% PEG 3350. |