5vgr | pdb_00005vgr
From Proteopedia
Structural highlights
Disease[ATLA3_HUMAN] Hereditary sensory and autonomic neuropathy type 1. The disease is caused by mutations affecting the gene represented in this entry. Function[ATLA3_HUMAN] GTPase tethering membranes through formation of trans-homooligomers and mediating homotypic fusion of endoplasmic reticulum membranes. Functions in endoplasmic reticulum tubular network biogenesis.[1] [2] References
| ||||||||||||||||||
This page was last modified 15:51, 17 May 2017.