6GWS
Crystal structure of human PCNA in complex with three p15 peptides
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ELETTRA BEAMLINE 5.2R |
| Synchrotron site | ELETTRA |
| Beamline | 5.2R |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-10-30 |
| Detector | DECTRIS PILATUS 2M |
| Wavelength(s) | 1.00 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 79.240, 89.750, 85.130 |
| Unit cell angles | 90.00, 117.25, 90.00 |
Refinement procedure
| Resolution | 75.690 - 2.900 |
| R-factor | 0.203 |
| Rwork | 0.200 |
| R-free | 0.26320 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1vym |
| RMSD bond length | 0.020 |
| RMSD bond angle | 2.396 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0135) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 89.750 | 8.560 | 3.080 |
| High resolution limit [Å] | 2.900 | 6.110 | 2.900 |
| Rmerge | 0.105 | 0.064 | |
| Rmeas | 0.090 | ||
| Number of reflections | 42698 | 2948 | 6844 |
| <I/σ(I)> | 4.77 | 10.04 | 0.73 |
| Completeness [%] | 92.2 | 93.4 | 91.3 |
| Redundancy | 1.768 | 1.846 | 1.762 |
| CC(1/2) | 0.986 | 0.986 | 0.763 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7 | 291 | 28% PEG 400, 0.2 M CaCl2, 0.1 M Hepes |






