9NKK
Horse liver alcohol dehydrogenase T178A in complex with NADH and N-cylcohexyl formamide
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRL BEAMLINE BL12-1 |
| Synchrotron site | SSRL |
| Beamline | BL12-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2025-01-30 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.979 |
| Spacegroup name | P 1 |
| Unit cell lengths | 43.804, 49.817, 92.465 |
| Unit cell angles | 93.05, 102.79, 108.27 |
Refinement procedure
| Resolution | 43.990 - 1.440 |
| R-factor | 0.1687 |
| Rwork | 0.167 |
| R-free | 0.20570 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.791 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.19.2_4158: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 43.990 | 1.520 |
| High resolution limit [Å] | 1.440 | 1.440 |
| Rmerge | 0.071 | 0.606 |
| Rmeas | 0.087 | 0.774 |
| Rpim | 0.050 | 0.475 |
| Total number of observations | 236143 | 26983 |
| Number of reflections | 95034 | 12032 |
| <I/σ(I)> | 4.9 | 2.2 |
| Completeness [%] | 73.8 | |
| Redundancy | 2.5 | 2.2 |
| CC(1/2) | 0.994 | 0.478 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8 | 277 | PEG400, 50mM Tris-HCl Buffer at pH8, co crystallized with 4mM NADH and 20mM CXF. Protein at 25 mg /mL |






