Summary: Death effector domain
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Death effector domain Edit Wikipedia article
| Death effector domain | |||||||||
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| structure of the FADD (Mort1) death-effector domain.[1] | |||||||||
| Identifiers | |||||||||
| Symbol | DED | ||||||||
| Pfam | PF01335 | ||||||||
| InterPro | IPR001875 | ||||||||
| SMART | DED | ||||||||
| PROSITE | PS50168 | ||||||||
| SCOP | 1a1z | ||||||||
| SUPERFAMILY | 1a1z | ||||||||
| CDD | cd00045 | ||||||||
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The death-effector domain (DED) is a protein interaction domain found to regulate a variety of cellular signalling pathways.[2] The DED domain is found in inactive procaspases (cysteine proteases) and proteins that regulate caspase activation in the apoptosis cascade such as FAS-associating death domain-containing protein (FADD). FADD recruits procaspase 8 and procaspase 10 into a death induced signaling complex (DISC). This recruitment is mediated by a homotypic interaction between the procaspase DED and a second DED that is death effector domain in an adaptor protein that is directly associated with activated TNF receptors. Complex formation allows proteolytic activation of procaspase into the active caspase form which results in the initiation of apoptosis (cell death). Structurally the DED domain are a subclass of protein motif known as the death fold and contains 6 alpha helices, that closely resemble the structure of the Death domain.
[edit] References
- ^ Eberstadt M, Huang B, Chen Z, et al. (April 1998). "NMR structure and mutagenesis of the FADD (Mort1) death-effector domain". Nature 392 (6679): 941–5. doi:10.1038/31972. PMID 9582077.
- ^ Valmiki MG, Ramos JW (March 2009). "Death effector domain-containing proteins". Cell. Mol. Life Sci. 66 (5): 814–30. doi:10.1007/s00018-008-8489-0. PMID 18989622.
[edit] External links
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This tab holds the annotation information that is stored in the Pfam database. As we move to using Wikipedia as our main source of annotation, the contents of this tab will be gradually replaced by the Wikipedia tab.
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Literature references
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Eberstadt M, Huang B, Chen Z, Meadows RP, Ng SC, Zheng L, Lenardo MJ, Fesik SW; , Nature 1998;392:941-945.: NMR structure and mutagenesis of the FADD (Mort1) death-effector domain. PUBMED:9582077 EPMC:9582077
External database links
| PANDIT: | PF01335 |
| PROSITE profile: | PS50168 |
| Pseudofam: | PF01335 |
| SCOP: | 1a1z |
| SMART: | DED |
| SYSTERS: | DED |
This tab holds annotation information from the InterPro database.
InterPro entry IPR001875
The death effector domain (DED) is a homotypic protein interaction module composed of a bundle of six alpha-helices. DED is related in sequence and structure to the death domain (DD, see INTERPRO) and the caspase recruitment domain (CARD, see INTERPRO), which work in similar pathways and show similar interaction properties [PUBMED:11504623]. The dimerisation of DED domains is mediated primarily by electrostatic interactions. DED domains can be found in isolation, or in combination with other domains. Domains associated with DED include: caspase catalytic domains (in caspase-8, -10), death domains (in FADD), nuclear localisation sequences (in DEDD), transmembrane domains (in Bap31 and Bar), nucleotide-binding domains (in Dap3), coiled-coil domains (in Hip and Hippi), SAM domains (in Bar), and E2-binding RING domains (in Bar) [PUBMED:15226512].
Several DED-containing proteins are involved in the regulation of apoptosis through their interactions with DED-containing caspases (INTERPRO), such as caspases 8 and 10 in humans, both of which contain tandem pairs of DEDs. There are many DED-containing modulators of apoptosis, which can either enhance or inhibit caspase activation [PUBMED:15173180].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | protein binding (GO:0005515) |
| Biological process | regulation of apoptotic process (GO:0042981) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Pfam Clan
Alignments
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| Seed (37) |
Full (947) |
Representative proteomes | NCBI (826) |
Meta (0) |
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| RP15 (158) |
RP35 (186) |
RP55 (257) |
RP75 (419) |
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| Jalview | ||||||||
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| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
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| Seed (37) |
Full (947) |
Representative proteomes | NCBI (826) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (158) |
RP35 (186) |
RP55 (257) |
RP75 (419) |
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| Raw Stockholm | ||||||||
| Gzipped | ||||||||
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
External links
MyHits provides a collection of tools to handle multiple sequence alignments. For example, one can refine a seed alignment (sequence addition or removal, re-alignment or manual edition) and then search databases for remote homologs using HMMER3.
HMM logo
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Trees
This page displays the phylogenetic tree for this family's seed alignment. We use FastTree to calculate neighbour join trees with a local bootstrap based on 100 resamples (shown next to the tree nodes). FastTree calculates approximately-maximum-likelihood phylogenetic trees from our seed alignment.
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Curation and family details
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Curation
| Seed source: | Bateman A |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Bateman A, Finn RD |
| Number in seed: | 37 |
| Number in full: | 947 |
| Average length of the domain: | 81.10 aa |
| Average identity of full alignment: | 24 % |
| Average coverage of the sequence by the domain: | 27.28 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 84 | ||||||||||||
| Family (HMM) version: | 16 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the DED domain has been found. There are 20 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein seqence.
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Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence