9UD7
Crystal structure of human glutaminyl cyclase in complex with Inhibitor CL7
This is a non-PDB format compatible entry.
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL19U1 |
| Synchrotron site | SSRF |
| Beamline | BL19U1 |
| Temperature [K] | 195 |
| Detector technology | PIXEL |
| Collection date | 2024-12-10 |
| Detector | DECTRIS PILATUS3 X CdTe 1M |
| Wavelength(s) | 0.97946 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 159.430, 181.570, 89.740 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 71.824 - 2.490 |
| R-factor | 0.1614 |
| Rwork | 0.160 |
| R-free | 0.22990 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3pbb |
| RMSD bond length | 0.032 |
| RMSD bond angle | 1.483 |
| Data reduction software | xia2 |
| Data scaling software | xia2 |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 71.824 | 71.850 | 2.530 |
| High resolution limit [Å] | 2.490 | 6.760 | 2.490 |
| Rmerge | 0.275 | ||
| Rmeas | 0.286 | ||
| Number of reflections | 91785 | 4885 | 4534 |
| <I/σ(I)> | 9.6 | ||
| Completeness [%] | 99.9 | ||
| Redundancy | 13.1 | ||
| CC(1/2) | 0.998 | 0.604 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 293 | 12% to 25% PEG 4000;0.2 M MgCl2;0.1 M Tris-HCL pH 8.0 |






