6fae | pdb_00006fae
From Proteopedia
The Sec7 domain of IQSEC2 (Brag1) in complex with the small GTPase Arf1
| ||||||||||||
Structural highlights
Disease[IQEC2_HUMAN] Severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome;X-linked non-syndromic intellectual disability. The disease is caused by mutations affecting the gene represented in this entry. Function[IQEC2_HUMAN] Is a guanine nucleotide exchange factor for the ARF GTP-binding proteins.[1] [ARF1_HUMAN] GTP-binding protein that functions as an allosteric activator of the cholera toxin catalytic subunit, an ADP-ribosyltransferase. Involved in protein trafficking among different compartments. Modulates vesicle budding and uncoating within the Golgi complex. Deactivation induces the redistribution of the entire Golgi complex to the endoplasmic reticulum, suggesting a crucial role in protein trafficking. In its GTP-bound form, its triggers the association with coat proteins with the Golgi membrane. The hydrolysis of ARF1-bound GTP, which is mediated by ARFGAPs proteins, is required for dissociation of coat proteins from Golgi membranes and vesicles. References
| ||||||||||||||||||
This page was last modified 07:11, 17 January 2018.