5HI1
Backbone Modifications in the Protein GB1 Helix: Aib24, beta-3-Lys28, beta-3-Lys31, Aib35
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU FR-E SUPERBRIGHT |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-04-22 |
Detector | RIGAKU SATURN 944 |
Wavelength(s) | 1.5418 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 74.371, 73.430, 79.436 |
Unit cell angles | 90.00, 99.35, 90.00 |
Refinement procedure
Resolution | 41.150 - 2.150 |
R-factor | 0.2174 |
Rwork | 0.214 |
R-free | 0.25180 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2qmt |
RMSD bond length | 0.008 |
RMSD bond angle | 1.074 |
Data reduction software | d*TREK |
Data scaling software | d*TREK |
Phasing software | PHENIX |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.150 | 2.230 |
High resolution limit [Å] | 2.150 | 2.150 |
Rmerge | 0.137 | 0.239 |
Number of reflections | 22880 | |
<I/σ(I)> | 15.9 | 4.2 |
Completeness [%] | 99.2 | 93.2 |
Redundancy | 11.4 | 3.04 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 298 | 0.2 M ammonium sulfate, 0.1M sodium acetate pH 4.5, 20% (w/v) PEG 4000 |