5HDM
Crystal structure of Arabidopsis thaliana glutamate-1-semialdehyde-2,1-aminomutase
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL17U |
| Synchrotron site | SSRF |
| Beamline | BL17U |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2015-07-15 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.9793 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 64.117, 109.331, 115.502 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 28.875 - 1.250 |
| R-factor | 0.1275 |
| Rwork | 0.126 |
| R-free | 0.14980 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2gsa |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.091 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.10.1_2155: ???) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 1.290 |
| High resolution limit [Å] | 1.250 | 2.690 | 1.250 |
| Rmerge | 0.050 | 0.031 | 0.320 |
| Rmeas | 0.057 | 0.035 | 0.370 |
| Rpim | 0.026 | 0.016 | 0.181 |
| Total number of observations | 829276 | ||
| Number of reflections | 212729 | ||
| <I/σ(I)> | 11 | ||
| Completeness [%] | 95.0 | 87.8 | 96 |
| Redundancy | 3.9 | 4.4 | 3.7 |
| CC(1/2) | 0.998 | 0.916 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 277 | potassium bromide, PEG 2000 MME |






