2f1s: Difference between revisions

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[[Image:2f1s.gif|left|200px]]
{{Seed}}
[[Image:2f1s.png|left|200px]]


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{{STRUCTURE_2f1s|  PDB=2f1s  |  SCENE=  }}  
{{STRUCTURE_2f1s|  PDB=2f1s  |  SCENE=  }}  


'''Crystal Structure of a Viral FLIP MC159'''
===Crystal Structure of a Viral FLIP MC159===




==Overview==
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Death receptor signaling is initiated by the assembly of the death-inducing signaling complex, which culminates in the activation of the initiator caspase, either caspase-8 or caspase-10. A family of viral and cellular proteins, known as FLIP, plays an essential role in the regulation of death receptor signaling. Viral FLIP (v-FLIP) and short cellular FLIP (c-FLIPS) inhibit apoptosis by interfering with death receptor signaling. The structure and mechanisms of v-FLIP and c-FLIPS remain largely unknown. Here we report a high resolution crystal structure of MC159, a v-FLIP derived from the molluscum contagiosum virus, which is a member of the human poxvirus family. Unexpectedly, the two tandem death effector domains (DEDs) of MC159 rigidly associate with each other through a hydrophobic interface. Structure-based sequence analysis suggests that this interface is conserved in the tandem DEDs from other v-FLIP, c-FLIPS, and caspase-8 and -10. Strikingly, the overall packing arrangement between the two DEDs of MC159 resembles that between the caspase recruitment domains of Apaf-1 and caspase-9. In addition, each DED of MC159 contains a highly conserved binding motif on the surface, to which loss-of-function mutations in MC159 map. These observations, in conjunction with published evidence, reveal significant insights into the function of v-FLIP and suggest a mechanism by which v-FLIP and c-FLIPS inhibit death receptor signaling.
The line below this paragraph, {{ABSTRACT_PUBMED_16317000}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_16317000}}


==About this Structure==
==About this Structure==
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[[Category: Disc]]
[[Category: Disc]]
[[Category: Flip]]
[[Category: Flip]]
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