5TIH
Structural basis for inhibition of erythrocyte invasion by antibodies to Plasmodium falciparum protein CyRPA
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2016-08-19 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.954 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 79.950, 87.380, 145.140 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 38.339 - 2.440 |
| R-factor | 0.1898 |
| Rwork | 0.189 |
| R-free | 0.21150 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5l9d |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.576 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 38.339 | 38.339 | 2.580 |
| High resolution limit [Å] | 2.440 | 7.230 | 2.440 |
| Rmerge | 0.081 | 0.035 | 0.991 |
| Rmeas | 0.089 | 0.038 | 1.088 |
| Total number of observations | 228722 | ||
| Number of reflections | 38349 | 1571 | 5742 |
| <I/σ(I)> | 14.54 | 34.5 | 2.17 |
| Completeness [%] | 99.4 | 96.4 | 97.8 |
| Redundancy | 5.964 | 5.391 | 5.619 |
| CC(1/2) | 0.998 | 0.999 | 0.727 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 5.5 | 298 | 11% PEG5000 monomethyl ether 0.2M NaAc |






