2b9i
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(New page: 200px<br /><applet load="2b9i" size="450" color="white" frame="true" align="right" spinBox="true" caption="2b9i, resolution 2.5Å" /> '''Crystal structure of ...)
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Revision as of 06:32, 21 November 2007
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Crystal structure of Fus3 with a docking motif from Msg5
Overview
Cells use a network of mitogen-activated protein kinases (MAPKs) to, coordinate responses to diverse extracellular signals. Here, we examine, the role of docking interactions in determining connectivity of the yeast, MAPKs Fus3 and Kss1. These closely related kinases are activated by the, common upstream MAPK kinase Ste7 yet generate distinct output responses, mating and filamentous growth, respectively. We find that docking, interactions are necessary for communication with the kinases and that, they can encode subtle differences in pathway-specific input and output., The cell cycle arrest mediator Far1, a mating-specific substrate, has a, docking motif that selectively binds Fus3. In contrast, the shared partner, Ste7 has a promiscuous motif that binds both Fus3 and Kss1. Structural, analysis reveals that Fus3 interacts with specific and promiscuous, peptides in conformationally distinct modes. Induced fit recognition may, allow docking peptides to achieve discrimination by exploiting subtle, differences in kinase flexibility.
About this Structure
2B9I is a Single protein structure of sequence from Saccharomyces cerevisiae with MG and ADP as ligands. Active as Non-specific serine/threonine protein kinase, with EC number 2.7.11.1 Full crystallographic information is available from OCA.
Reference
The role of docking interactions in mediating signaling input, output, and discrimination in the yeast MAPK network., Remenyi A, Good MC, Bhattacharyya RP, Lim WA, Mol Cell. 2005 Dec 22;20(6):951-62. PMID:16364919
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