6K26
Crystal structure of Vibrio cholerae methionine aminopeptidase
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | ROTATING ANODE |
| Source details | RIGAKU MICROMAX-007 HF |
| Temperature [K] | 100 |
| Detector technology | IMAGE PLATE |
| Collection date | 2017-06-12 |
| Detector | RIGAKU RAXIS IV++ |
| Wavelength(s) | 1.542 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 49.529, 50.010, 131.086 |
| Unit cell angles | 90.00, 97.25, 90.00 |
Refinement procedure
| Resolution | 34.660 - 1.850 |
| R-factor | 0.1679 |
| Rwork | 0.166 |
| R-free | 0.20760 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2mat |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.626 |
| Data reduction software | HKL-2000 (v716) |
| Data scaling software | HKL-2000 (v716) |
| Phasing software | MOLREP (11.6.03) |
| Refinement software | REFMAC (5.8.0238) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 40.000 | 40.000 | 1.920 |
| High resolution limit [Å] | 1.850 | 3.980 | 1.850 |
| Rmerge | 0.083 | 0.042 | 0.531 |
| Rmeas | 0.101 | 0.051 | 0.648 |
| Rpim | 0.057 | 0.029 | 0.366 |
| Total number of observations | 155933 | ||
| Number of reflections | 53682 | 5567 | 5260 |
| <I/σ(I)> | 8.9 | ||
| Completeness [%] | 98.5 | 98.7 | 97.8 |
| Redundancy | 2.9 | 2.9 | 2.8 |
| CC(1/2) | 0.997 | 0.618 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 298 | 0.1M Hepes, 12 % PEG 3350 |






