Atlastin: Difference between revisions

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== Disease ==
== Disease ==


Defects in the ATN gene are a cause of spastic paraplegia type 3.
Defects in the ATN gene are a cause of the degenerative spinal cord disorder spastic paraplegia type 3.


== Relevance ==
== Relevance ==

Revision as of 10:15, 8 November 2015

<StructureSection load='4ido' size='340' side='right' caption='Structure of human atlastin cytoplasmic domain complex with GDP and AlF4 (PDB code 4ido).' scene=>

Function

Atlastin (ATN) is a GTPase and a Golgi body transmembrane protein. ATN was shown to be required in membrane fusion and ER formation in Drosophila melanogaster.

Disease

Defects in the ATN gene are a cause of the degenerative spinal cord disorder spastic paraplegia type 3.

Relevance

Structural highlights

3D structures of atlastin

Updated on 08-November-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