8DSV
The structure of NicA2 in complex with N-methylmyosmine
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-G |
Synchrotron site | APS |
Beamline | 21-ID-G |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2022-02-04 |
Detector | RAYONIX MX-300 |
Wavelength(s) | 0.9787 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 75.080, 86.700, 152.130 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 57.180 - 2.500 |
R-factor | 0.1669 |
Rwork | 0.165 |
R-free | 0.21180 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 7c4a |
RMSD bond length | 0.004 |
RMSD bond angle | 0.641 |
Data reduction software | MOSFLM |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 57.180 | 2.600 |
High resolution limit [Å] | 2.500 | 2.500 |
Number of reflections | 34120 | 3430 |
<I/σ(I)> | 11.7 | 5.2 |
Completeness [%] | 97.2 | |
Redundancy | 7 | |
CC(1/2) | 0.894 | 0.879 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 277 | 0.2 M ammonium citrate tribasic, pH 7.0, 20% PEG3350 |