6QFV
Human carbonic anhydrase II with bound IrCp* complex (cofactor 8) to generate an artificial transfer hydrogenase (ATHase)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06DA |
Synchrotron site | SLS |
Beamline | X06DA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-09-30 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1.000 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 42.396, 41.680, 72.353 |
Unit cell angles | 90.00, 104.40, 90.00 |
Refinement procedure
Resolution | 41.100 - 1.450 |
R-factor | 0.1569 |
Rwork | 0.156 |
R-free | 0.16740 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3zp9 |
RMSD bond length | 0.015 |
RMSD bond angle | 2.386 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.680 | 1.470 |
High resolution limit [Å] | 1.450 | 1.450 |
Rmerge | 0.063 | 0.473 |
Number of reflections | 43249 | 2208 |
<I/σ(I)> | 14.8 | 2.8 |
Completeness [%] | 96.7 | 71.1 |
Redundancy | 6 | 3.1 |
CC(1/2) | 0.998 | 0.488 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.9 | 293 | 2.6 M ammonium sulfate, 50 mM Tris-H2SO4 |