5BWI
Crystallographic structure of a bacterial heparanase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-10-22 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.954 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 125.030, 125.030, 125.160 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 31.290 - 1.600 |
R-factor | 0.16563 |
Rwork | 0.164 |
R-free | 0.19187 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3vnz |
RMSD bond length | 0.009 |
RMSD bond angle | 1.321 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0073) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 31.290 |
High resolution limit [Å] | 1.600 |
Number of reflections | 129599 |
<I/σ(I)> | 6.9 |
Completeness [%] | 99.4 |
Redundancy | 14.54 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.8 M potassium sodium tartrate tetrahydrate |