4O7X
Crystal structure of human ALKBH5 in complex with Mn2+
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 130 |
Detector technology | CCD |
Collection date | 2012-03-06 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 1.0 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 57.093, 57.093, 145.729 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.000 - 1.780 |
R-factor | 0.2154 |
Rwork | 0.214 |
R-free | 0.23762 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4nrm |
RMSD bond length | 0.006 |
RMSD bond angle | 1.057 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | BALBES |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 53.160 | 1.830 |
High resolution limit [Å] | 1.780 | 1.780 |
Number of reflections | 23830 | |
Completeness [%] | 99.3 | 97 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5 | 289 | 20% PEG 4K, 100mM CH3CO2NH4, 100mM Na-citrate, pH 5, VAPOR DIFFUSION, HANGING DROP, temperature 289K |