7M3X
Crystal Structure of the Apo Form of Human RBBP7
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-E |
Synchrotron site | APS |
Beamline | 24-ID-E |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2021-02-13 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.97918 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 44.726, 88.775, 97.165 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.630 - 1.460 |
R-factor | 0.171 |
Rwork | 0.170 |
R-free | 0.19250 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3cfs |
RMSD bond length | 0.007 |
RMSD bond angle | 1.446 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 1.490 |
High resolution limit [Å] | 1.460 | 3.960 | 1.460 |
Rmerge | 0.074 | 0.035 | 0.777 |
Rmeas | 0.078 | 0.037 | 0.829 |
Rpim | 0.023 | 0.011 | 0.286 |
Total number of observations | 727132 | ||
Number of reflections | 68121 | 3687 | 3354 |
<I/σ(I)> | 7 | ||
Completeness [%] | 99.9 | 99.9 | 99.8 |
Redundancy | 10.7 | 10.2 | 8.1 |
CC(1/2) | 0.999 | 0.805 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.8 | 293 | 28%(w/v)PEG3350 MME, 0.2M NaCl, 0.1M Hepes pH7.8, 5% MPD, 5% Glycerol |