2pzx: Difference between revisions

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[[Image:2pzx.jpg|left|200px]]
{{Seed}}
[[Image:2pzx.png|left|200px]]


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{{STRUCTURE_2pzx|  PDB=2pzx  |  SCENE=  }}  
{{STRUCTURE_2pzx|  PDB=2pzx  |  SCENE=  }}  


'''Structure of the methuselah ectodomain with peptide inhibitor'''
===Structure of the methuselah ectodomain with peptide inhibitor===




==Overview==
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G protein-coupled receptors (GPCRs) mediate signaling from extracellular ligands to intracellular signal transduction proteins. Methuselah (Mth) is a class B (secretin-like) GPCR, a family typified by their large, ligand-binding, N-terminal extracellular domains. Downregulation of mth increases the life span of Drosophila melanogaster; inhibitors of Mth signaling should therefore enhance longevity. We used mRNA display selection to identify high-affinity (K(d) = 15 to 30 nM) peptide ligands that bind to the N-terminal ectodomain of Mth. The selected peptides are potent antagonists of Mth signaling, and structural studies suggest that they perturb the interface between the Mth ecto- and transmembrane domains. Flies constitutively expressing a Mth antagonist peptide have a robust life span extension, which suggests that the peptides inhibit Mth signaling in vivo. Our work thus provides new life span-extending ligands for a metazoan and a general approach for the design of modulators of this important class of GPCRs.
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{{ABSTRACT_PUBMED_17546039}}


==About this Structure==
==About this Structure==
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[[Category: Gpcr g protein-coupled receptor ectodomain]]
[[Category: Gpcr g protein-coupled receptor ectodomain]]
[[Category: Signaling protein]]
[[Category: Signaling protein]]
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