5F3X
Crystal structure of Harmonin NPDZ1 in complex with ANKS4B SAM-PBM
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-01-14 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97915 |
Spacegroup name | P 32 |
Unit cell lengths | 124.566, 124.566, 49.654 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 31.511 - 2.649 |
R-factor | 0.2291 |
Rwork | 0.227 |
R-free | 0.26440 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3k1r |
RMSD bond length | 0.008 |
RMSD bond angle | 0.994 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 31.511 | 2.700 |
High resolution limit [Å] | 2.649 | 2.650 |
Number of reflections | 24978 | |
<I/σ(I)> | 38.2 | 2.9 |
Completeness [%] | 99.5 | 100 |
Redundancy | 5.7 | 5.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 289 | 3.0 M NaCl, 0.1 M Bis-tris |