6ODC
Crystal structure of HDAC8 in complex with compound 30
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2017-01-06 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.99 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 87.540, 91.161, 92.574 |
Unit cell angles | 90.00, 94.07, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.800 |
R-factor | 0.19642 |
Rwork | 0.194 |
R-free | 0.23577 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1t64 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.452 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0158) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.900 |
High resolution limit [Å] | 2.800 | 2.800 |
Rmerge | 0.013 | |
Number of reflections | 35823 | 3547 |
<I/σ(I)> | 14.8 | 1.5 |
Completeness [%] | 99.8 | 99.9 |
Redundancy | 3.4 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.3 | 291 | 0.1M MES pH5.3, 5% PEG6000, 0.14 M Gly-Gly-Gly, 2mM TCEP |