Atlastin: Difference between revisions
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Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}} | Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}} | ||
{{#tree:id=OrganizedByTopic|openlevels=0| | |||
*Atlastin-1 | |||
**[[3q5d]], [[3q5e]], [[3qnu]], [[3qof]] – hATN cytoplasmic domain + GDP – human<br /> | |||
**[[6b9d]], [[6b9e]] – hATN cytoplasmic domain (mutant) + GDP <br /> | |||
**[[4idn]] – hATN cytoplasmic domain + GNP <br /> | |||
**[[4idp]] – hATN cytoplasmic domain (mutant) + GNP <br /> | |||
**[[4ido]] – hATN cytoplasmic domain + GDP + AlF4<br /> | |||
**[[4idq]], [[6b9f]] – hATN cytoplasmic domain (mutant) + GDP + AlF4<br /> | |||
**[[3x1d]] – ATN + GDP – ''Drosophila melanogaster''<br /> | |||
*Atlastin-3 | |||
**[[5vgr]] – hATN cytoplasmic domain + GDP <br /> | |||
}} | |||
== References == | == References == | ||
<references/> | <references/> | ||
[[Category: Topic Page]] | [[Category: Topic Page]] |
Revision as of 14:12, 22 March 2018
FunctionAtlastin (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.[1] DiseaseDefects in the ATN gene are a cause of the degenerative spinal cord disorder spastic paraplegia type 3 and of hereditary sensory neuropathy type 1D. Structural highlights |
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3D structures of atlastin3D structures of atlastin
Updated on 22-March-2018
ReferencesReferences
- ↑ 1.0 1.1 Byrnes LJ, Singh A, Szeto K, Benvin NM, O'Donnell JP, Zipfel WR, Sondermann H. Structural basis for conformational switching and GTP loading of the large G protein atlastin. EMBO J. 2013 Jan 18. doi: 10.1038/emboj.2012.353. PMID:23334294 doi:http://dx.doi.org/10.1038/emboj.2012.353