1UMJ
Crystal structure of Pyrococcus horikoshii CutA in the presence of 3M guanidine hydrochloride
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL38B1 |
Synchrotron site | SPring-8 |
Beamline | BL38B1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2003-03-13 |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 0.9 |
Spacegroup name | P 3 |
Unit cell lengths | 53.210, 53.210, 59.665 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 20.000 - 1.600 |
Rwork | 0.214 |
R-free | 0.25300 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1j2v |
RMSD bond length | 0.017 |
RMSD bond angle | 1.700 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | AMoRE |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.000 | 1.660 |
High resolution limit [Å] | 1.600 | 1.600 |
Number of reflections | 24828 | |
<I/σ(I)> | 19.9 | |
Completeness [%] | 99.6 | 100 |
Redundancy | 3.9 | 3.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Oil batch method | 4 | 293 | Acetate buffer (pH 4.0), PEG4000, Ammonium sulfate, 3M guanidine hydrochloride, Oil batch method, temperature 293K |