6L05
Crystal structure of uPA_H99Y in complex with 50F
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX II BEAMLINE I911-2 |
Synchrotron site | MAX II |
Beamline | I911-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-09-03 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.987 |
Spacegroup name | H 3 |
Unit cell lengths | 120.430, 120.430, 42.680 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 22.760 - 2.490 |
R-factor | 0.179 |
Rwork | 0.175 |
R-free | 0.26100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4dva |
RMSD bond length | 0.010 |
RMSD bond angle | 1.784 |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0257) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 22.760 | 2.530 |
High resolution limit [Å] | 2.490 | 2.490 |
Rmerge | 0.112 | 0.049 |
Number of reflections | 8025 | 1538 |
<I/σ(I)> | 9.3 | |
Completeness [%] | 99.3 | |
Redundancy | 3.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 298 | 50mM sodium citrate at pH 4.6, 1.95M (NH4)2SO4, 0.03% NaN3, 5% PEG 400 |