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Atlastin

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Defects in the ATN gene are a cause of the degenerative spinal cord disorder spastic paraplegia type 3 and of hereditary sensory neuropathy type 1D.
Defects in the ATN gene are a cause of the degenerative spinal cord disorder spastic paraplegia type 3 and of hereditary sensory neuropathy type 1D.
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</StructureSection>
==3D structures of atlastin==
==3D structures of atlastin==

Revision as of 07:59, 3 December 2015

Structure of human atlastin cytoplasmic domain complex with GDP and AlF4 (PDB code 4ido).

Drag the structure with the mouse to rotate

3D structures of atlastin

Updated on 03-December-2015

3q5d, 3q5e, 3qnu, 3qof – hATN cytoplasmic domain + GDP – human
4idn – hATN cytoplasmic domain + GNP
4idp – hATN cytoplasmic domain (mutant) + GNP
4ido – hATN cytoplasmic domain + GDP + AlF4
4idq – hATN cytoplasmic domain (mutant) + GDP + AlF4


References

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky

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