6NZ3
Crystal structure of computationally designed protein XAA_GGHN
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.3.1 |
Synchrotron site | ALS |
Beamline | 8.3.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-09-16 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 1.1111 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 88.741, 51.271, 85.873 |
Unit cell angles | 90.00, 110.08, 90.00 |
Refinement procedure
Resolution | 80.655 - 2.300 |
R-factor | 0.2641 |
Rwork | 0.262 |
R-free | 0.30170 |
Structure solution method | MOLECULAR REPLACEMENT |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHENIX |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 80.660 | 1.720 |
High resolution limit [Å] | 1.660 | 1.660 |
Rmerge | 0.035 | |
Rmeas | 0.039 | |
Rpim | 0.015 | |
Number of reflections | 34486 | 1008 |
<I/σ(I)> | 14.4 | 0.3 |
Completeness [%] | 80.7 | 23.64 |
Redundancy | 5.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 10.5 | 291.15 | 0.1 M CAPS pH 10.5, 40% (v/v) MPD |