2DQT
High resolution crystal structure of the complex of the hydrolytic antibody Fab 6D9 and a transition-state analog
Replaces: 1HYXExperimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-6A |
Synchrotron site | Photon Factory |
Beamline | BL-6A |
Temperature [K] | 293 |
Detector technology | IMAGE PLATE |
Collection date | 1994-05-01 |
Detector | FUJI |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 55.906, 61.662, 66.673 |
Unit cell angles | 90.00, 104.68, 90.00 |
Refinement procedure
Resolution | 6.000 - 1.800 |
R-factor | 0.187 |
Rwork | 0.187 |
R-free | 0.24600 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2igf |
RMSD bond length | 0.008 |
RMSD bond angle | 1.500 |
Data reduction software | PROTEIN |
Data scaling software | WEIS |
Phasing software | X-PLOR |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 6.000 | 2.000 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.070 | |
Number of reflections | 28513 | |
Completeness [%] | 69.0 | 44 |
Redundancy | 6.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8.3 | THE PRE-FORMED COMPLEX WAS CRYSTALLIZED FROM 17% PEG 4000, 50MM TRIS, 0.1MM EDTA, PH 8.3 |