9CSX
matrix metalloproteinase-10 proenzyme
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | NSLS-II BEAMLINE 17-ID-1 |
| Synchrotron site | NSLS-II |
| Beamline | 17-ID-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2022-07-30 |
| Detector | DECTRIS EIGER X 9M |
| Wavelength(s) | 1.0 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 80.841, 72.003, 54.495 |
| Unit cell angles | 90.00, 130.82, 90.00 |
Refinement procedure
| Resolution | 27.120 - 1.670 |
| R-factor | 0.19 |
| Rwork | 0.189 |
| R-free | 0.21260 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.008 |
| RMSD bond angle | 0.968 |
| Data reduction software | autoPROC |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.621 | 1.697 |
| High resolution limit [Å] | 1.669 | 1.669 |
| Rmerge | 0.159 | 0.986 |
| Rmeas | 0.197 | |
| Rpim | 0.115 | 0.731 |
| Number of reflections | 25894 | 1322 |
| <I/σ(I)> | 2.8 | 0.8 |
| Completeness [%] | 94.1 | |
| Redundancy | 2.6 | |
| CC(1/2) | 0.985 | 0.339 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 298 | 0.2 M zinc acetate, 0.1 M imidazole, pH 7.5 and 17 % (w/v)PEG 3000, 4.0 % (v/v) acetonitrile |






