1r8s
From Proteopedia
|
ARF1[DELTA1-17]-GDP IN COMPLEX WITH A SEC7 DOMAIN CARRYING THE MUTATION OF THE CATALYTIC GLUTAMATE TO LYSINE
Overview
Small GTP-binding (G) proteins are activated by GDP/GTP nucleotide, exchange stimulated by guanine nucleotide exchange factors (GEFs)., Nucleotide dissociation from small G protein-GEF complexes involves, transient GDP-bound intermediates whose structures have never been, described. In the case of Arf proteins, small G proteins that regulate, membrane traffic in eukaryotic cells, such intermediates can be trapped, either by the natural inhibitor brefeldin A or by charge reversal at the, catalytic glutamate of the Sec7 domain of their GEFs. Here we report the, crystal structures of these intermediates that show that membrane, recruitment of Arf and nucleotide dissociation are separate reactions, stimulated by Sec7. The reactions proceed through sequential rotations of, the Arf.GDP core towards the Sec7 catalytic site, and are blocked by, interfacial binding of brefeldin A and unproductive stabilization of GDP, by charge reversal. The structural characteristics of the reaction and its, modes of inhibition reveal unexplored ways in which to inhibit the, activation of small G proteins.
About this Structure
1R8S is a Protein complex structure of sequences from Bos taurus and Homo sapiens with SO4, SO3, GDP, BME and FMT as ligands. Full crystallographic information is available from OCA.
Reference
Structural snapshots of the mechanism and inhibition of a guanine nucleotide exchange factor., Renault L, Guibert B, Cherfils J, Nature. 2003 Dec 4;426(6966):525-30. PMID:14654833
Page seeded by OCA on Mon Nov 12 19:01:26 2007
Categories: Bos taurus | Homo sapiens | Protein complex | Cherfils, J. | Guibert, B. | Renault, L. | BME | FMT | GDP | SO3 | SO4 | Protein transport/exchange factor
