5IBZ
Crystal structure of a novel cyclase (pfam04199).
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-12-03 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9794 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 64.508, 120.618, 148.822 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 38.814 - 1.611 |
R-factor | 0.1342 |
Rwork | 0.133 |
R-free | 0.16140 |
Structure solution method | SAD |
RMSD bond length | 0.009 |
RMSD bond angle | 1.331 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | HKL-3000 |
Refinement software | PHENIX (dev_1888) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 38.814 | 1.640 |
High resolution limit [Å] | 1.611 | 1.611 |
Rmerge | 0.083 | 0.484 |
Number of reflections | 150117 | |
<I/σ(I)> | 17 | 2.8 |
Completeness [%] | 99.9 | 98.5 |
Redundancy | 5.9 | 4.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 2KMME 30%, Tris pH 8 0.1M, NH4Acet 0.2M |