6Y74
X-ray crystal structure of human carbonic anhydrase IX catalytic domain.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX IV BEAMLINE BioMAX |
Synchrotron site | MAX IV |
Beamline | BioMAX |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-05-08 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.979 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 113.930, 78.340, 74.320 |
Unit cell angles | 90.00, 128.22, 90.00 |
Refinement procedure
Resolution | 37.130 - 1.530 |
R-factor | 0.1751 |
Rwork | 0.174 |
R-free | 0.19840 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3iai |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.17.1_3660) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 37.130 | 1.560 |
High resolution limit [Å] | 1.530 | 1.530 |
Rmerge | 0.110 | 0.815 |
Number of reflections | 75610 | 3288 |
<I/σ(I)> | 10.6 | 2.2 |
Completeness [%] | 98.3 | |
Redundancy | 6.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 4.3 | 293 | 17% PEG 6000, 1.4 M Sodium citrate pH 4.3, 1 M LiCl |