5TDQ
Crystal Structure of the GOLD domain of ACBD3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CLSI BEAMLINE 08ID-1 |
Synchrotron site | CLSI |
Beamline | 08ID-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-08-18 |
Detector | RAYONIX MX-300 |
Wavelength(s) | 0.9797 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 55.510, 55.510, 140.150 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 46.717 - 2.493 |
R-factor | 0.2398 |
Rwork | 0.238 |
R-free | 0.26170 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4tlg |
RMSD bond length | 0.009 |
RMSD bond angle | 1.151 |
Data reduction software | iMOSFLM |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 46.720 |
High resolution limit [Å] | 2.493 |
Rmerge | 0.059 |
Number of reflections | 5907 |
<I/σ(I)> | 8.6 |
Completeness [%] | 62.9 |
Redundancy | 4.5 |
CC(1/2) | 0.998 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 289 | 13% PEG 4000, 200 mM Ammonium Sulfate, 100 mM HEPES, 10% 2-propanol, 10% glycerol |