2UWE
Large CDR3a loop alteration as a function of MHC mutation
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-BM |
Synchrotron site | APS |
Beamline | 22-BM |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-03-03 |
Detector | MARRESEARCH |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 93.489, 84.178, 121.773 |
Unit cell angles | 90.00, 92.05, 90.00 |
Refinement procedure
Resolution | 121.000 - 2.400 |
R-factor | 0.243 |
Rwork | 0.240 |
R-free | 0.29000 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1lp9 |
RMSD bond length | 0.006 |
RMSD bond angle | 1.040 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | REFMAC |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.490 |
High resolution limit [Å] | 2.400 | 2.370 |
Rmerge | 0.060 | 0.350 |
Number of reflections | 76682 | |
<I/σ(I)> | 8.3 | 1.64 |
Completeness [%] | 83.9 | 67.2 |
Redundancy | 2.76 | 2.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.8 | 14% PEG 8000, 1 M NACL, 25 MM HEPES, PH 7.8 |