2rg8

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{{STRUCTURE_2rg8| PDB=2rg8 | SCENE= }}
{{STRUCTURE_2rg8| PDB=2rg8 | SCENE= }}
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'''Crystal Structure of Programmed for Cell Death 4 Middle MA3 domain'''
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===Crystal Structure of Programmed for Cell Death 4 Middle MA3 domain===
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==Overview==
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Programmed Cell Death 4 (PDCD4) is a protein known to bind eukaryotic initiation factor 4A (eIF4A), inhibit translation initiation, and act as a tumor suppressor. PDCD4 contains two C-terminal MA3 domains, which are thought to be responsible for its inhibitory function. Here, we analyze the structures and inhibitory functions of these two PDCD4 MA3 domains by x-ray crystallography, NMR, and surface plasmon resonance. We show that both MA3 domains are structurally and functionally very similar and bind specifically to the eIF4A N-terminal domain (eIF4A-NTD) using similar binding interfaces. We found that the PDCD4 MA3 domains compete with the eIF4G MA3 domain and RNA for eIF4A binding. Our data provide evidence that PDCD4 inhibits translation initiation by displacing eIF4G and RNA from eIF4A. The PDCD4 MA3 domains act synergistically to form a tighter and more stable complex with eIF4A, which explains the need for two tandem MA3 domains.
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{{ABSTRACT_PUBMED_18296639}}
==About this Structure==
==About this Structure==
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[[Category: Rna-binding]]
[[Category: Rna-binding]]
[[Category: Translation]]
[[Category: Translation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 16:51:28 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 22:57:18 2008''

Revision as of 19:57, 27 July 2008

Image:2rg8.png

Template:STRUCTURE 2rg8

Crystal Structure of Programmed for Cell Death 4 Middle MA3 domain

Template:ABSTRACT PUBMED 18296639

About this Structure

2RG8 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

PDCD4 inhibits translation initiation by binding to eIF4A using both its MA3 domains., Suzuki C, Garces RG, Edmonds KA, Hiller S, Hyberts SG, Marintchev A, Wagner G, Proc Natl Acad Sci U S A. 2008 Feb 22;. PMID:18296639

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