2D5A
hypothetical protein from Pyrococcus horikoshii OT3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL41XU |
Synchrotron site | SPring-8 |
Beamline | BL41XU |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-07-25 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 1.0 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 70.118, 70.118, 141.712 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 37.480 - 1.700 |
Rwork | 0.225 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.035 |
RMSD bond angle | 2.600 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.760 |
High resolution limit [Å] | 1.700 | 1.700 |
Rmerge | 0.038 | 0.639 |
Number of reflections | 23416 | |
<I/σ(I)> | 31.919 | 2.5 |
Completeness [%] | 98.8 | 88.1 |
Redundancy | 17.2 | 6.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293 | 30% PEG 4000, 0.1M Tris-HCl, 0.2M Sodium Fluoride, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K |