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Structure of the guanine nucleotide exchange factor Sec7 domain of human arno and analysis of the interaction with ARF GTPase.
- 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.
- Subjects :
- ADP-Ribosylation Factor 1
ADP-Ribosylation Factors
Amino Acid Sequence
Binding Sites
Crystallography, X-Ray
GTP-Binding Proteins genetics
Guanosine Diphosphate metabolism
Humans
Molecular Sequence Data
Mutagenesis, Site-Directed
Sequence Analysis
Sequence Deletion
Sequence Homology, Amino Acid
Fungal Proteins chemistry
GTP Phosphohydrolases metabolism
GTP-Binding Proteins chemistry
GTP-Binding Proteins metabolism
GTPase-Activating Proteins
Guanine Nucleotide Exchange Factors
Protein Structure, Tertiary
Subjects
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