8GSM
Crystal Structure of VibMO1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2021-12-08 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9792 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 120.430, 127.780, 146.450 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.140 - 2.880 |
R-factor | 0.236 |
Rwork | 0.234 |
R-free | 0.29310 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5eow |
RMSD bond length | 0.010 |
RMSD bond angle | 1.169 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.18.1_3865) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.980 |
High resolution limit [Å] | 2.880 | 2.880 |
Rmerge | 0.175 | 0.768 |
Rpim | 0.094 | 0.613 |
Number of reflections | 52795 | 5019 |
<I/σ(I)> | 21.15 | 3.02 |
Completeness [%] | 99.0 | 98 |
Redundancy | 9.3 | 9.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | Sodium bromide , PEG 3350 |