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 |