3C2A
Antibody Fab fragment 447-52D in complex with UG1033 peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL11-1 |
Synchrotron site | SSRL |
Beamline | BL11-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2002-08-25 |
Detector | ADSC QUANTUM 315 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 70.251, 76.482, 114.130 |
Unit cell angles | 90.00, 101.49, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.100 |
R-factor | 0.2413 |
Rwork | 0.240 |
R-free | 0.29775 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1q1j |
RMSD bond length | 0.017 |
RMSD bond angle | 1.637 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.150 |
High resolution limit [Å] | 2.100 | 2.100 |
Number of reflections | 60586 | |
<I/σ(I)> | 27.1 | 4 |
Completeness [%] | 85.7 | 86 |
Redundancy | 5.1 | 4.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.9 | 298 | 1.58M ammonium sulfate 0.1M Tris 1mM CuCl2, pH 7.9, VAPOR DIFFUSION, SITTING DROP, temperature 298K |