8GXN
The crystal structure of CsFAOMT2 in complex with SAH
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CAMD BEAMLINE GCPCC |
Synchrotron site | CAMD |
Beamline | GCPCC |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2021-10-29 |
Detector | DECTRIS PILATUS 300K |
Wavelength(s) | 0.978690 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 74.688, 74.688, 81.523 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 30.060 - 1.340 |
R-factor | 0.1644 |
Rwork | 0.164 |
R-free | 0.17080 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3c3y |
RMSD bond length | 0.008 |
RMSD bond angle | 1.201 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 64.740 | 1.350 |
High resolution limit [Å] | 1.280 | 1.280 |
Number of reflections | 61963 | 7996 |
<I/σ(I)> | 33.6 | |
Completeness [%] | 90.6 | |
Redundancy | 15 | |
CC(1/2) | 1.000 | 0.898 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 289 | 1.5M Ammonium Sulfate, 100 mM Sodium Citrate pH5.5 |