2YHF
1.9 Angstrom Crystal Structure of CLEC5A
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SRS BEAMLINE PX10.1 |
Synchrotron site | SRS |
Beamline | PX10.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-11-02 |
Detector | MARMOSAIC 225 mm CCD |
Spacegroup name | P 31 |
Unit cell lengths | 109.109, 109.109, 84.879 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 94.490 - 1.900 |
R-factor | 0.219 |
Rwork | 0.216 |
R-free | 0.26727 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ENTRIES 1K9J 3bdw 1e87 2it5 3BC6. |
RMSD bond length | 0.007 |
RMSD bond angle | 0.947 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | BALBES |
Refinement software | REFMAC (5.3.0002) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.970 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.070 | 0.500 |
Number of reflections | 88632 | |
<I/σ(I)> | 12.9 | 1.62 |
Completeness [%] | 87.1 | 76.4 |
Redundancy | 2.9 | 2.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | 100MM TRIS PH8.0, 30% PEG 6000 |