6FCM
Crystal structure of human PCNA
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE MASSIF-1 |
| Synchrotron site | ESRF |
| Beamline | MASSIF-1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2016-10-29 |
| Detector | DECTRIS PILATUS3 X 2M |
| Wavelength(s) | 0.96600 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 39.180, 140.060, 169.970 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 45.000 - 2.800 |
| R-factor | 0.19917 |
| Rwork | 0.195 |
| R-free | 0.27588 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1axc |
| RMSD bond length | 0.008 |
| RMSD bond angle | 1.310 |
| Data reduction software | XDS (VERSION May 1, 2016 BUILT=20160617) |
| Data scaling software | XSCALE (VERSION May 1, 2016 BUILT=20160617) |
| Phasing software | PHASER (2.6.1) |
| Refinement software | REFMAC (5.8.0158) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 45.000 | 2.870 |
| High resolution limit [Å] | 2.800 | 2.800 |
| Rmerge | 0.048 | 0.802 |
| Rmeas | 0.056 | 0.962 |
| Number of reflections | 23289 | 1567 |
| <I/σ(I)> | 18.27 | |
| Completeness [%] | 97.0 | 92.2 |
| Redundancy | 3.43 | 3.03 |
| CC(1/2) | 0.999 | 0.719 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 293 | 19 to 23% PEG 3350, 0.2 to 0.3 M NaCl, 0.1 M Tris-HCl pH 8.5 |






