Crystal structure of the R482W mutant of lamin A/C

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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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Crystal structure of the R482W mutant of lamin A/C

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