6V8N
Crystal structure of the p300 acetyltransferase domain with AcCoA competitive inhibitor 17
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CLSI BEAMLINE 08ID-1 |
Synchrotron site | CLSI |
Beamline | 08ID-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-05-23 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.97949 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 45.650, 104.820, 169.120 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 52.460 - 2.300 |
R-factor | 0.2028 |
Rwork | 0.200 |
R-free | 0.24710 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | internal |
RMSD bond length | 0.012 |
RMSD bond angle | 1.796 |
Data reduction software | XDS |
Data scaling software | Aimless (0.5.21) |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 52.460 | 52.460 | 2.360 |
High resolution limit [Å] | 2.300 | 10.290 | 2.300 |
Rmerge | 0.106 | 0.048 | 1.304 |
Rmeas | 0.115 | 0.054 | 1.408 |
Total number of observations | 129190 | ||
Number of reflections | 18495 | 256 | 1324 |
<I/σ(I)> | 11.4 | 28.02 | 1.37 |
Completeness [%] | 99.6 | 96.6 | 99.8 |
Redundancy | 6.985 | 5.496 | 7.08 |
CC(1/2) | 0.997 | 0.994 | 0.489 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5.5 | 277 | 0.2 M Ammonium Sulfate, 0.1 M BisTris pH 5.5, 20% PEG 3350, streak-seed with loop |