5W1O
Crystal Structure of HPV16 L1 Pentamer Bound to Heparin Oligosaccharides
This is a non-PDB format compatible entry.
Replaces: 3OAEExperimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.2.2 |
Synchrotron site | ALS |
Beamline | 8.2.2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-10-04 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.98 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 96.620, 101.252, 128.182 |
Unit cell angles | 90.00, 90.63, 90.00 |
Refinement procedure
Resolution | 47.430 - 2.800 |
R-factor | 0.226 |
Rwork | 0.224 |
R-free | 0.27000 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2r5h |
RMSD bond length | 0.016 |
RMSD bond angle | 1.469 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | PHENIX (1.8.4_1496) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.426 | 2.900 |
High resolution limit [Å] | 2.797 | 2.800 |
Rmerge | 0.082 | 0.353 |
Number of reflections | 60092 | |
<I/σ(I)> | 14.28 | |
Completeness [%] | 98.5 | |
Redundancy | 2.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 291 | 30% PEG400, 0.1 M MES |