9FQB
crystal structure of ClY21-HNP1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PETRA III, EMBL c/o DESY BEAMLINE P14 (MX2) |
Synchrotron site | PETRA III, EMBL c/o DESY |
Beamline | P14 (MX2) |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2024-02-29 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.97625 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 46.075, 46.075, 51.282 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 31.490 - 1.090 |
R-factor | 0.1115 |
Rwork | 0.111 |
R-free | 0.12180 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.015 |
RMSD bond angle | 1.595 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 31.492 | 1.109 |
High resolution limit [Å] | 1.090 | 1.090 |
Rmerge | 0.079 | |
Number of reflections | 26621 | 1252 |
<I/σ(I)> | 18.9 | |
Completeness [%] | 99.6 | |
Redundancy | 17.6 | |
CC(1/2) | 0.999 | 0.909 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.1 M imidazole, 1.0 M sodium acetate, pH 6.5 |