7BYQ
The mutant variant of PNGM-1. H279A was substituted for alanine to study metal coordination.
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PAL/PLS BEAMLINE 5C (4A) |
| Synchrotron site | PAL/PLS |
| Beamline | 5C (4A) |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2013-05-08 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.97940 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 121.380, 83.057, 163.581 |
| Unit cell angles | 90.00, 110.69, 90.00 |
Refinement procedure
| Resolution | 49.040 - 1.960 |
| R-factor | 0.5205 |
| Rwork | 0.519 |
| R-free | 0.55680 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6j4n |
| RMSD bond length | 0.006 |
| RMSD bond angle | 1.447 |
| Data reduction software | DENZO |
| Data scaling software | SCALEPACK |
| Phasing software | HKL-3000 |
| Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 1.990 |
| High resolution limit [Å] | 1.940 | 5.320 | 1.960 |
| Rmerge | 0.122 | 0.076 | 0.397 |
| Rmeas | 0.134 | 0.083 | 0.452 |
| Rpim | 0.055 | 0.032 | 0.209 |
| Number of reflections | 211626 | 10958 | 10432 |
| <I/σ(I)> | 5.1 | ||
| Completeness [%] | 96.6 | 97.2 | 95.6 |
| Redundancy | 5.1 | 6.3 | 4.1 |
| CC(1/2) | 0.996 | 0.716 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 5.4 | 287 | 0.1 M Sodium acetate, 1.5 M Sodium formate, 0.08 M CaCl2 and 10% PEG 3350 |






