6AYA
Structure of the native full-length HIV-1 capsid protein in complex with Nup153 peptide
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 4.2.2 |
| Synchrotron site | ALS |
| Beamline | 4.2.2 |
| Temperature [K] | 100 |
| Detector technology | CMOS |
| Collection date | 2016-12-01 |
| Detector | RDI CMOS_8M |
| Wavelength(s) | 1.000031 |
| Spacegroup name | P 6 |
| Unit cell lengths | 92.544, 92.544, 58.288 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 36.241 - 2.400 |
| R-factor | 0.2358 |
| Rwork | 0.234 |
| R-free | 0.27360 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4xfx |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.508 |
| Data reduction software | Aimless (0.5.32) |
| Data scaling software | Aimless (0.5.32) |
| Phasing software | PHASER (2.7.17) |
| Refinement software | PHENIX (1.11.1-2575_1692) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 36.241 | 36.240 | 2.490 |
| High resolution limit [Å] | 2.400 | 8.980 | 2.400 |
| Rmerge | 0.065 | 0.032 | 0.689 |
| Rmeas | 0.068 | 0.034 | 0.723 |
| Rpim | 0.021 | 0.011 | 0.220 |
| Number of reflections | 10941 | 220 | 1168 |
| <I/σ(I)> | 24.7 | ||
| Completeness [%] | 97.2 | 94.2 | 100 |
| Redundancy | 10.6 | 9.8 | 10.8 |
| CC(1/2) | 0.999 | 0.998 | 0.901 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 291 | PEG3350, NaI, MIB, Glycerol |






