5F1I
MHC with 9-mer peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2015-05-12 |
Detector | BIODIFF |
Wavelength(s) | 0.9793 |
Spacegroup name | P 1 |
Unit cell lengths | 84.101, 94.626, 124.355 |
Unit cell angles | 84.60, 72.79, 81.61 |
Refinement procedure
Resolution | 41.545 - 2.904 |
R-factor | 0.2101 |
Rwork | 0.208 |
R-free | 0.24030 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2xpg |
RMSD bond length | 0.009 |
RMSD bond angle | 1.480 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASES |
Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 2.696 |
Number of reflections | 97116 |
<I/σ(I)> | 6.322 |
Completeness [%] | 97.9 |
Redundancy | 2.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 291 | 0.2 M potassium thiocyanate, pH 7.0, 20% PEG 3350 (w/v), 30% 1,4-Dioxane (v/v) |