6OR4
Crystal structure of SpGH29
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 | 2015-05-28 |
Detector | RAYONIX MX-300 |
Wavelength(s) | 0.9795 |
Spacegroup name | P 1 |
Unit cell lengths | 49.960, 68.820, 72.670 |
Unit cell angles | 76.58, 73.24, 73.61 |
Refinement procedure
Resolution | 46.590 - 2.100 |
R-factor | 0.1721 |
Rwork | 0.169 |
R-free | 0.23190 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3eyp |
RMSD bond length | 0.006 |
RMSD bond angle | 1.371 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.590 | 2.160 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.062 | 0.344 |
Rpim | 0.062 | 0.344 |
Number of reflections | 50203 | 4093 |
<I/σ(I)> | 14.1 | 3.5 |
Completeness [%] | 98.0 | 96.9 |
Redundancy | 3.9 | 4 |
CC(1/2) | 0.998 | 0.895 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 291 | 20 % PEG 3350, 0.2 M NaCl, 1 mM DTT and 0.1 M Tris. |