3HAH
Crystal structure of human PACSIN1 F-BAR domain (C2 lattice)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X29A |
Synchrotron site | NSLS |
Beamline | X29A |
Temperature [K] | 110 |
Detector technology | CCD |
Collection date | 2008-10-30 |
Detector | ADSC QUANTUM 210 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 160.009, 85.457, 88.392 |
Unit cell angles | 90.00, 117.56, 90.00 |
Refinement procedure
Resolution | 48.070 - 2.770 |
R-factor | 0.2169 |
Rwork | 0.215 |
R-free | 0.26010 |
Structure solution method | SAD |
RMSD bond length | 0.006 |
RMSD bond angle | 0.998 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | SHELXS |
Refinement software | PHENIX ((phenix.refine)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.070 | 3.000 |
High resolution limit [Å] | 2.770 | 2.770 |
<I/σ(I)> | 9.9 | 2.5 |
Completeness [%] | 27.5 | |
Redundancy | 2.6 | 3.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.4 | 293 | 0.2M potassium sodium tartrate tetrahydrate, 20% PEG 3350, pH 7.4, VAPOR DIFFUSION, HANGING DROP, temperature 293K |