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Structure of the guanine nucleotide exchange factor Sec7 domain of human arno and analysis of the interaction with ARF GTPase.

Authors :
Mossessova E
Gulbis JM
Goldberg J
Source :
Cell [Cell] 1998 Feb 06; Vol. 92 (3), pp. 415-23.
Publication Year :
1998

Abstract

Sec7-related guanine nucleotide exchange factors (GEFs) initiate vesicle budding from the Golgi membrane surface by converting the GTPase ARF to a GTP-bound, membrane-associated form. Here we report the crystal structure of the catalytic Sec7 homology domain of Arno, a human GEF for ARF1, determined at 2.2 angstroms resolution. The Sec7 domain is an elongated, all-helical protein with a distinctive hydrophobic groove that is phylogenetically conserved. Structure-based mutagenesis identifies the groove and an adjacent conserved loop as the ARF-interacting surface. The sites of Sec7 domain interaction on ARF1 have subsequently been mapped, by protein footprinting experiments, to the switch 1 and switch 2 GTPase regions, leading to a model for the interaction between ARF GTPases and Sec7 domain exchange factors.

Details

Language :
English
ISSN :
0092-8674
Volume :
92
Issue :
3
Database :
MEDLINE
Journal :
Cell
Publication Type :
Academic Journal
Accession number :
9476900
Full Text :
https://doi.org/10.1016/s0092-8674(00)80933-2