Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2012-10-18 |
| Detector | ADSC QUANTUM 315 |
| Spacegroup name | H 3 2 |
| Unit cell lengths | 129.230, 129.230, 233.791 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 43.180 - 3.100 |
| R-factor | 0.16604 |
| Rwork | 0.164 |
| R-free | 0.20891 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3ZGR |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.144 |
| Data reduction software | XDS |
| Data scaling software | SCALA |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.7.0032) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 43.100 | 3.260 |
| High resolution limit [Å] | 3.090 | 3.090 |
| Rmerge | 0.140 | 0.620 |
| Number of reflections | 13929 | |
| <I/σ(I)> | 12.9 | 3.6 |
| Completeness [%] | 99.5 | 96.5 |
| Redundancy | 9.7 | 9.2 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | 7 | THE PROTEIN WAS DIALYSED AGAINST HEPES BUFFER WITH BARBITURIC ACID, THE FINAL CONCENTRATION OF PROTEIN WAS 2 MG/ML AND THIS WAS SET UP IN A 1:1 RATIO AGAINST 180 MM NACL, 31% V/V PEG 400 AND 100 MM HEPES PH 7.0. |
