5LJT
Crystal structure of human carbonic anhydrase II in complex with the 4-((1-phenyl-1H-1,2,3-triazol-4-yl)methoxy)benzenesulfonamide inhibitor
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID23-1 |
| Synchrotron site | ESRF |
| Beamline | ID23-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2015-07-16 |
| Detector | DECTRIS PILATUS 6M-F |
| Wavelength(s) | 0.9762 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 42.363, 41.400, 72.171 |
| Unit cell angles | 90.00, 104.41, 90.00 |
Refinement procedure
| Resolution | 30.000 - 1.000 |
| R-factor | 0.1391 |
| Rwork | 0.138 |
| R-free | 0.15720 |
| Structure solution method | FOURIER SYNTHESIS |
| Starting model (for MR) | 4fik |
| RMSD bond length | 0.005 |
| RMSD bond angle | 1.189 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | REFMAC |
| Refinement software | REFMAC (5.8.0073) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 41.400 | 41.400 | 1.060 |
| High resolution limit [Å] | 1.000 | 3.000 | 1.000 |
| Rmerge | 0.060 | 0.037 | 0.672 |
| Number of reflections | 121936 | ||
| <I/σ(I)> | 10.22 | 33.68 | 1.3 |
| Completeness [%] | 93.7 | 98.6 | 75.6 |
| Redundancy | 3.5 | 2.6 | |
| CC(1/2) | 0.998 | 0.997 | 0.520 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 8 | 296 | 1.5 M sodium citrate, Tris 50 mM |






