9NXJ
The GH43 domain of an alpha-l-arabinofuranosidase (AtAbf43C_GH43) from Acetivibrio thermocellus DSM1313
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 | 2024-09-25 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 0.92015 |
Spacegroup name | P 65 |
Unit cell lengths | 105.304, 105.304, 128.856 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.590 - 2.320 |
R-factor | 0.2049 |
Rwork | 0.203 |
R-free | 0.24690 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.008 |
RMSD bond angle | 0.992 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.17_3644) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 29.590 | 2.380 |
High resolution limit [Å] | 2.320 | 2.320 |
Rmerge | 0.118 | 0.852 |
Rmeas | 0.121 | 0.874 |
Rpim | 0.027 | 0.192 |
Total number of observations | 724982 | 50475 |
Number of reflections | 35192 | 2503 |
<I/σ(I)> | 21.2 | 3.3 |
Completeness [%] | 99.7 | |
Redundancy | 20.6 | 20.2 |
CC(1/2) | 0.999 | 0.867 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5.5 | 293 | PEGmme 5000, pH 5.5 Bis-Tris, AmS04 |