3NA1
Crystal structure of human CYP11A1 in complex with 20-hydroxycholesterol
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 23-ID-B |
Synchrotron site | APS |
Beamline | 23-ID-B |
Temperature [K] | 100 |
Collection date | 2009-11-18 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 82.810, 115.149, 85.727 |
Unit cell angles | 90.00, 101.45, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.250 |
R-factor | 0.195 |
Rwork | 0.193 |
R-free | 0.23200 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3n9y |
RMSD bond length | 0.009 |
RMSD bond angle | 1.177 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Refinement software | REFMAC (5.5.0102) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 2.290 |
High resolution limit [Å] | 2.250 | 6.100 | 2.250 |
Rmerge | 0.072 | 0.031 | 0.223 |
Number of reflections | 74265 | ||
<I/σ(I)> | 15.3 | ||
Completeness [%] | 99.3 | 99.7 | 96.2 |
Redundancy | 4.5 | 4.6 | 4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 291 | PEG 8000, Ca acetate, pH 7.5, vapor diffusion, hanging drop, temperature 291K |