5E6G
Crystal Structure of De Novo Designed Protein CA01
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-BM |
Synchrotron site | APS |
Beamline | 22-BM |
Temperature [K] | 63 |
Detector technology | CCD |
Collection date | 2014-06-14 |
Detector | MAR CCD 130 mm |
Wavelength(s) | 1 |
Spacegroup name | H 3 |
Unit cell lengths | 116.537, 116.537, 57.215 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 37.850 - 2.090 |
R-factor | 0.202 |
Rwork | 0.200 |
R-free | 0.23400 |
RMSD bond length | 0.003 |
RMSD bond angle | 0.616 |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.4_1496) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 58.270 |
High resolution limit [Å] | 2.090 |
Number of reflections | 17000 |
<I/σ(I)> | 13.8 |
Completeness [%] | 98.6 |
Redundancy | 3.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 293.15 | 0.1M Tris:HCL, pH 8.5 - 1.0M Ammonium Phosphate Dibasic |