4OK4
Crystal Structure of Alg17c Mutant H202L
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-G |
Synchrotron site | APS |
Beamline | 21-ID-G |
Temperature [K] | 77 |
Detector technology | CCD |
Collection date | 2013-06-11 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.97857 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 86.470, 127.153, 88.277 |
Unit cell angles | 90.00, 111.20, 90.00 |
Refinement procedure
Resolution | 25.000 - 1.700 |
R-factor | 0.19443 |
Rwork | 0.193 |
R-free | 0.21665 |
Structure solution method | SAD |
RMSD bond length | 0.005 |
RMSD bond angle | 0.999 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | SHARP |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.000 | 1.744 |
High resolution limit [Å] | 1.700 | 1.700 |
Number of reflections | 191532 | |
Completeness [%] | 98.1 | 87.47 |
Redundancy | 4.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 289 | 0.1 M Tris, 5% 2-methyl-2,4-pentanediol (MPD), 10% Polyethylene glycol (PEG) 6000, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 289K |