| Literature DB >> 9604936 |
E B Fauman1, J P Cogswell, B Lovejoy, W J Rocque, W Holmes, V G Montana, H Piwnica-Worms, M J Rink, M A Saper.
Abstract
Cdc25 phosphatases activate the cell division kinases throughout the cell cycle. The 2.3 A structure of the human Cdc25A catalytic domain reveals a small alpha/beta domain with a fold unlike previously described phosphatase structures but identical to rhodanese, a sulfur-transfer protein. Only the active-site loop, containing the Cys-(X)5-Arg motif, shows similarity to the tyrosine phosphatases. In some crystals, the catalytic Cys-430 forms a disulfide bond with the invariant Cys-384, suggesting that Cdc25 may be self-inhibited during oxidative stress. Asp-383, previously proposed to be the general acid, instead serves a structural role, forming a conserved buried salt-bridge. We propose that Glu-431 may act as a general acid. Structure-based alignments suggest that the noncatalytic domain of the MAP kinase phosphatases will share this topology, as will ACR2, a eukaryotic arsenical resistance protein.Entities:
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Year: 1998 PMID: 9604936 DOI: 10.1016/s0092-8674(00)81190-3
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582