4AT3
CRYSTAL STRUCTURE OF TRKB KINASE DOMAIN IN COMPLEX WITH CPD5N
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-2 |
Synchrotron site | ESRF |
Beamline | ID14-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-04-16 |
Detector | ADSC CCD |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 86.331, 94.340, 46.037 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 24.870 - 1.770 |
R-factor | 0.2 |
Rwork | 0.197 |
R-free | 0.22440 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4asz |
RMSD bond length | 0.007 |
RMSD bond angle | 0.940 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | BUSTER (2.9.7) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.190 | 1.810 |
High resolution limit [Å] | 1.770 | 1.770 |
Rmerge | 0.070 | 0.330 |
Number of reflections | 37068 | |
<I/σ(I)> | 12.3 | 2 |
Completeness [%] | 99.0 | 94.8 |
Redundancy | 4.1 | 2.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6 | 277 | THE TRKB-CPD5N COMPLEX WAS OBTAINED BY COCRYSTALLIZATION IN 1.6 M AMMONIUM SULFATE, 50 MM MES, PH 6.0 AT 4 DEGREESC IN PRESENCE OF 2 MM OF INHIBITOR. |