3QBT
Crystal structure of OCRL1 540-678 in complex with Rab8a:GppNHp
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 | 2009-09-18 |
Detector | MARMOSAIC 225 mm CCD |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 157.147, 55.340, 173.836 |
Unit cell angles | 90.00, 91.93, 90.00 |
Refinement procedure
Resolution | 47.378 - 2.000 |
R-factor | 0.2096 |
Rwork | 0.208 |
R-free | 0.24110 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | codes 1r2q 2qv2 |
RMSD bond length | 0.014 |
RMSD bond angle | 1.412 |
Data scaling software | XSCALE |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.378 | 2.100 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.055 | 0.334 |
Number of reflections | 99857 | |
<I/σ(I)> | 4.2 | |
Completeness [%] | 98.3 | 97 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.6 | 293 | 20% (w/v) PEG 4000, 20% (v/v) glycerol, 0.16 M ammonium sulphate, 0.1 M sodium acetate, pH 4.6, vapor diffusion, hanging drop, temperature 293K |