8SE1
Structure of Full-length Human Protein Kinase C Beta 2 (PKCBII) in the Inactive Conformation
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-C |
| Synchrotron site | APS |
| Beamline | 24-ID-C |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2021-04-20 |
| Detector | DECTRIS EIGER2 X 16M |
| Wavelength(s) | 0.979180 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 130.556, 89.098, 160.714 |
| Unit cell angles | 90.00, 107.05, 90.00 |
Refinement procedure
| Resolution | 48.750 - 3.320 |
| R-factor | 0.2018 |
| Rwork | 0.199 |
| R-free | 0.25550 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.605 |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.20.1) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 3.470 |
| High resolution limit [Å] | 3.320 | 7.210 | 3.350 |
| Rmerge | 0.070 | 0.070 | 0.962 |
| Rmeas | 0.352 | 0.083 | |
| Rpim | 0.044 | 0.582 | |
| Number of reflections | 25781 | 2636 | 2603 |
| <I/σ(I)> | 16 | ||
| Completeness [%] | 99.3 | 98.4 | 99.9 |
| Redundancy | 3.5 | 3.4 | 3.7 |
| CC(1/2) | 0.906 | 0.994 | 0.464 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 277.15 | PEG8000, MES buffer, magnesium chloride |






