5XKJ
Crystal structure of plant receptor ERL1-TMM in complexe with EPF2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17B1 |
Synchrotron site | SSRF |
Beamline | BL17B1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-10-30 |
Detector | BRUKER SMART 6000 |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 |
Unit cell lengths | 66.154, 65.601, 142.496 |
Unit cell angles | 102.86, 97.60, 93.58 |
Refinement procedure
Resolution | 46.186 - 3.475 |
R-factor | 0.2555 |
Rwork | 0.254 |
R-free | 0.27700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4mn8 |
RMSD bond length | 0.005 |
RMSD bond angle | 0.850 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.599 |
High resolution limit [Å] | 3.450 | 3.475 |
Number of reflections | 29462 | |
<I/σ(I)> | 6.8 | |
Completeness [%] | 93.8 | |
Redundancy | 3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 291 | 0.1 mM Ammonium citrate tribasic pH 7.0, 10% Polyethylene glycol 3350 |