3KPA
Ubiquitin fold modifier conjugating enzyme from Leishmania major (probable)
Experimental procedure
| Experimental method | MAD |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.2.2 |
| Synchrotron site | ALS |
| Beamline | 8.2.2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2003-08-12 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.9784 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 57.274, 34.133, 126.774 |
| Unit cell angles | 90.00, 99.32, 90.00 |
Refinement procedure
| Resolution | 50.000 - 2.200 |
| R-factor | 0.217 |
| Rwork | 0.214 |
| R-free | 0.27300 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2in1 |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.220 |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | BALBES |
| Refinement software | REFMAC |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.370 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Rmerge | 0.102 | 0.394 |
| Number of reflections | 23133 | |
| <I/σ(I)> | 11.4 | 2.2 |
| Completeness [%] | 91.4 | 70.1 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 6 | 293 | protein buffer 25 mM HEPES pH 7.5, 120 mM NaCl; crystallization buffer 100 mM Na Cacodylate, 300 mM Ammonium Sulfate,, 30% PEG 4000, vapor diffusion, temperature 293K |






