3PHD
Crystal structure of human HDAC6 in complex with ubiquitin
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 23-ID-B |
Synchrotron site | APS |
Beamline | 23-ID-B |
Detector technology | CCD |
Collection date | 2008-03-05 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 1.03317 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 133.748, 133.748, 118.768 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 32.720 - 3.000 |
R-factor | 0.2352 |
Rwork | 0.235 |
R-free | 0.26480 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3c5k |
RMSD bond length | 0.010 |
RMSD bond angle | 1.120 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP (9.2) |
Refinement software | BUSTER (2.8.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.050 |
High resolution limit [Å] | 3.000 | 3.000 |
Rmerge | 0.091 | 0.767 |
Number of reflections | 22204 | |
<I/σ(I)> | 45.8 | 4.7 |
Completeness [%] | 100.0 | 100 |
Redundancy | 16.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.6 | 297 | 15% PEG 3350, 0.1M Ammonium Sulphate, 0.1M Bis-Tris, pH 5.6, temperature 297K |