3RHG
Crystal structure of amidohydrolase pmi1525 (target efi-500319) from proteus mirabilis hi4320
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X29A |
Synchrotron site | NSLS |
Beamline | X29A |
Temperature [K] | 90 |
Detector technology | CCD |
Collection date | 2009-03-17 |
Detector | ADSC QUANTUM 315 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 101.203, 101.203, 65.614 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 50.000 - 1.530 |
R-factor | 0.12095 |
Rwork | 0.120 |
R-free | 0.15637 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3htw |
RMSD bond length | 0.010 |
RMSD bond angle | 1.227 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 90.000 | 1.560 |
High resolution limit [Å] | 1.530 | 1.530 |
Rmerge | 0.800 | |
Number of reflections | 58633 | |
<I/σ(I)> | 9.9 | 2.2 |
Completeness [%] | 99.7 | 95 |
Redundancy | 17.7 | 15.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6.5 | 0.1M SODIUM CACODYLATE, PH 6.5, 0.2M AMMONIUM SULFATE, 30% PEG8000, VAPOR DIFFUSION, SITTING DROP, TEMPERATURE 294K |