Atlastin: Difference between revisions
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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. | ||
<scene name='59/590828/Cv/4'> | == Structural highlights == | ||
*<scene name='59/590828/Cv/4'>GDP/AlF4 binding site</scene> | |||
</StructureSection> | </StructureSection> | ||
==3D structures of atlastin== | ==3D structures of atlastin== | ||
Revision as of 11:17, 10 December 2015
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3D structures of atlastin
Updated on 10-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
