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Crystal structure of the R482W mutant of lamin A/C
Autogenerated by
for
roshna_r
Created on Sat, 2019-07-13 11:23, last updated on Sat, 2019-07-13 11:23
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General Information
This Model was autogenerated from the
"Quick Submit"
tool.
Model ID
3DPX-011474
Category
Proteins, Macromolecules and Viruses
Keyword(s)
Immunoglobulin fold, lamin, Cardiomyopathy, Charcot-Marie-Tooth disease, Disease mutation, Intermediate filament, Limb-girdle muscular dystrophy, Lipoprotein, NUCLEUS, Phosphoprotein
Protein Data Bank ID
3GEF
Experimental Method
X-RAY DIFFRACTION
Resolution
1.5
Model Details
Associated Species
Escherichia coli
Oligomeric Details
monomeric
Scattering Type
x-ray
Attribution
PubMed ID
19 574 635
Digital Object Identifier (DOI)
10.1107/S1744309109020302
Citation Title
Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD).
Citation Year
2009
STL/VRML Files
PDB-3GEF-ribbon-secondary.wrl
PDB-3GEF-ribbon-rainbow.wrl
PDB-3GEF-ribbon-bychain.wrl
PDB-3GEF-ribbon.stl
PDB-3GEF-surf-bychain.wrl
PDB-3GEF-surf-hydropathy.wrl
PDB-3GEF-surf-coulombic.wrl
PDB-3GEF-surf.stl
PDB-3GEF.zip
X3D Files
PDB-3GEF-ribbon-secondary.x3d
PDB-3GEF-ribbon-rainbow.x3d
PDB-3GEF-ribbon-bychain.x3d
PDB-3GEF-ribbon.x3d
PDB-3GEF-surf-bychain.x3d
PDB-3GEF-surf-hydropathy.x3d
PDB-3GEF-surf-coulombic.x3d
PDB-3GEF-surf.x3d
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