7G7M
Crystal Structure of rat Autotaxin in complex with N-[(3,4-dichlorophenyl)methyl]-N-methyl-2-[4-oxo-6-[4-(1,3-thiazol-2-yl)piperazin-1-yl]quinazolin-3-yl]acetamide, i.e. SMILES N1=C(SC=C1)N1CCN(CC1)c1ccc2N=CN(CC(=O)N(C)Cc3ccc(c(c3)Cl)Cl)C(=O)c2c1 with IC50=0.0764342 microM
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-02-03 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 0.999930 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 84.073, 91.820, 120.696 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 45.910 - 1.690 |
R-factor | 0.1952 |
Rwork | 0.192 |
R-free | 0.25610 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | inhouse model |
RMSD bond length | 0.010 |
RMSD bond angle | 1.468 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0103) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 45.910 | 45.910 | 1.740 |
High resolution limit [Å] | 1.690 | 7.580 | 1.690 |
Rmerge | 0.132 | 0.105 | 2.590 |
Rmeas | 0.145 | 0.115 | 2.891 |
Total number of observations | 555052 | ||
Number of reflections | 100434 | 1296 | 6471 |
<I/σ(I)> | 6.26 | 15.61 | 0.62 |
Completeness [%] | 96.2 | 97.9 | 84.7 |
Redundancy | 5.527 | 5.863 | 4.887 |
CC(1/2) | 0.993 | 0.991 | 0.593 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 4.5 | 293 | 15.3 mg/mL protein in 20mM BICINE/NaOH pH8.5, 150mM NaCl, 0.02% NaN3 mixed 50-70% with 50-30% reservoir consisting of 11-17% PEG3350, 0.1M Na-acetate pH4.5, 0.2M Ca-acetate, total volume 200nL |