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2WEW

Crystal structure of human apoM in complex with myristic acid

Experimental procedure
Experimental methodMAD
Source typeSYNCHROTRON
Source detailsBESSY BEAMLINE 14.1
Synchrotron siteBESSY
Beamline14.1
Temperature [K]100
Detector technologyCCD
DetectorRAYONICS
Spacegroup nameP 43 21 2
Unit cell lengths49.940, 49.940, 144.670
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 1.950
R-factor0.21112
Rwork0.208
R-free0.26746
Structure solution methodMAD
Starting model (for MR)NONE
RMSD bond length0.015
RMSD bond angle1.610
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareSHELXCDE
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.060
High resolution limit [Å]1.9501.950
Rmerge0.0500.360
Number of reflections13952
<I/σ(I)>25.184.84
Completeness [%]98.491.3
Redundancy7.065.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
17.2ABOUT 1-2 MICROL OF PROTEIN (10-16 MG/ML IN 20 MM TRIS-HCL, PH 7.2) WERE MIXED WITH 1-2 MICROL OF 30 % PEG1500 (W/V, IN DEIONISED WATER) AND EQUILIBRATED AGAINST 700 MICROL OF RESERVOIR SOLUTION CONTAINING 30 % PEG1500.

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PDB entries from 2024-05-15

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