6SB7
Human Carbonic Anhydrase II in complex with fragment.
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | BESSY BEAMLINE 14.2 |
| Synchrotron site | BESSY |
| Beamline | 14.2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-03-10 |
| Detector | DECTRIS PILATUS3 S 2M |
| Wavelength(s) | 0.9184 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 42.497, 41.657, 72.496 |
| Unit cell angles | 90.00, 104.33, 90.00 |
Refinement procedure
| Resolution | 35.830 - 1.090 |
| R-factor | 0.1192 |
| Rwork | 0.118 |
| R-free | 0.13670 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3ks3 |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.107 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 41.660 | 1.160 |
| High resolution limit [Å] | 1.090 | 1.090 |
| Number of reflections | 98467 | 14806 |
| <I/σ(I)> | 13.47 | 4.5 |
| Completeness [%] | 97.2 | 91.1 |
| Redundancy | 3.61 | 3.48 |
| CC(1/2) | 0.998 | 0.930 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.8 | 291 | Ammonium sulfate 2.7 M, TRIS 0.1 M, saturated with para-Chloromercuribenzoic acid |
