6VJN
Structure of NHP D11A.B5Fab in complex with 16055 V2b peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2017-08-17 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 1.00 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 64.780, 74.780, 101.450 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.980 - 2.000 |
R-factor | 0.1829 |
Rwork | 0.180 |
R-free | 0.23640 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6rcs |
RMSD bond length | 0.011 |
RMSD bond angle | 1.107 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.960 | 2.050 |
High resolution limit [Å] | 2.000 | 2.000 |
Number of reflections | 33842 | 2389 |
<I/σ(I)> | 7.4 | |
Completeness [%] | 99.4 | |
Redundancy | 6.4 | |
CC(1/2) | 0.993 | 0.863 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 293 | 0.1 M Tris, pH 8.0, 1.32 M sodium/potasssium tartrate |