6OTX
Crystallographic Structure of (HbII-HbIII)-O2 from Lucina pectinata at pH 7.0
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL9-2 |
Synchrotron site | SSRL |
Beamline | BL9-2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-07-12 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.19499 |
Spacegroup name | P 42 21 2 |
Unit cell lengths | 74.736, 74.736, 152.571 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 33.558 - 2.539 |
R-factor | 0.1952 |
Rwork | 0.192 |
R-free | 0.24880 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3pt8 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | REFMAC |
Refinement software | PHENIX (1.13_2998) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.580 |
High resolution limit [Å] | 2.539 | 2.540 |
Number of reflections | 15012 | 784334 |
<I/σ(I)> | 36.6 | |
Completeness [%] | 99.6 | |
Redundancy | 10 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | COUNTER-DIFFUSION | 7 | 293 | Sodium Formate |