The isolated catalytic hairpin of the Ras-specific guanine nucleotide exchange factor Cdc25 Mm retains nucleotide dissociation activity but has impaired nucleotide exchange activity

Abstract

Cdc25 Mm is a mammalian Ras-specific guanine nucleotide exchange factor (GEF). By homology modeling we show that it shares with Sos-GEF the structure of the putative catalytic HI hairpin where the dominant negative T1184E mutation is located. Similarly to Cdc25 MmT1184E, the isolated wild-type and mutant hairpins retain the ability to displace Ras-bound nucleotide, originate a stable Ras/GEF complex and downregulate the Ras pathway in vivo. These results indicate that nucleotide re-entry and Ras/GEF dissociation – final steps in the GEF catalytic cycle – require GEF regions different from the HI hairpin. GEF down-sizing could lead to development of novel Ras inhibitors.