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 | 2006-07-12 |
| Detector | MARMOSAIC 225 mm CCD |
| Wavelength(s) | 0.9791 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 83.317, 83.317, 181.066 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 48.880 - 2.250 |
| R-factor | 0.2242 |
| Rwork | 0.222 |
| R-free | 0.25750 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1erk |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.460 |
| Data reduction software | XDS |
| Data scaling software | Aimless (0.7.4) |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 48.880 | 48.880 | 2.320 |
| High resolution limit [Å] | 2.250 | 9.000 | 2.250 |
| Rmerge | 0.156 | 0.098 | 2.484 |
| Rmeas | 0.164 | 0.108 | 2.613 |
| Rpim | 0.050 | 0.041 | 0.802 |
| Total number of observations | 5255 | 28538 | |
| Number of reflections | 31175 | 594 | 2803 |
| <I/σ(I)> | 10.6 | 23.8 | 2.1 |
| Completeness [%] | 100.0 | 99.5 | 100 |
| Redundancy | 10.7 | 8.8 | 10.2 |
| CC(1/2) | 0.857 | 0.867 | 0.562 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.7 | 277 | 1.8M MgSO4; 0.1M MES |






