56  structures 94  species 2  interactions 1116  sequences 147  architectures

Family: Death (PF00531)

Summary

Death domain Add an annotation

No Pfam abstract.


Literature references

  1. Hofmann K, Tschopp J; , FEBS lett 1995;371:321-323.: The death domain motif found in Fas (Apo-1) and Tnf receptor is Present in proteins involved in apoptosis and axonal guidance. PUBMED:7556620

  2. Feinstein E, Kimchi A, Wallach D, Boldin M, Varfolomeev E; , Trends Biochem Sci 1995;20:342-344.: The death domain - A module shared by proteins with diverse cellular functions. PUBMED:7482697

  3. Huang BH, Eberstadt M, Olejniczak ET, Meadows RP, Fesik SW; , Nature 1996;384:638-641.: NMR structure and mutagenesis of the Fas (Apo-1/CD95) death domain. PUBMED:8967952


InterPro entry IPR000488

The death domain (DD) is a homotypic protein interaction module composed of a bundle of six alpha-helices. DD is related in sequence and structure to the death effector domain (DED, see ) and the caspase recruitment domain (CARD, see ), which work in similar pathways and show similar interaction properties PUBMED:11504623. DD bind each other forming oligomers. Mammals have numerous and diverse DD-containing proteins PUBMED:7482697. Within these proteins, the DD domains can be found in combination with other domains, including: CARDs, DEDs, ankyrin repeats (), caspase-like folds, kinase domains, leucine zippers (), leucine-rich repeats (LRR) (), TIR domains (), and ZU5 domains () PUBMED:15226512.

Some DD-containing proteins are involved in the regulation of apoptosis and inflammation through their activation of caspases and NF-kappaB, which typically involves interactions with TNF (tumour necrosis factor) cytokine receptors PUBMED:14585074, PUBMED:14601641. In humans, eight of the over 30 known TNF receptors contain DD in their cytoplasmic tails; several of these TNF receptors use caspase activation as a signalling mechanism. The DD mediates self-association of these receptors, thus giving the signal to downstream events that lead to apoptosis. Other DD-containing proteins, such as ankyrin, MyD88 and pelle, are probably not directly involved in cell death signalling. DD-containing proteins also have links to innate immunity, communicating with Toll family receptors through bipartite adapter proteins such as MyD88 PUBMED:12691620.

Clan

This family is a member of clan Death (CL0041), which contains the following 4 members:

CARD Death DED PAAD_DAPIN

Gene Ontology

External database links

Domain organisation

Below is a listing of the unique domain organisations or architectures in which this domain is found. More...

Loading domain graphics...

Alignments

There are various ways to view or download the sequence alignments that we store. You can use a sequence viewer to look at either the seed or full alignment for the family, or you can look at a plain text version of the sequence in a variety of different formats. More...

View options

Alignment:
Viewer:  

Formatting options

Alignment:
Format:
Order:
Sequence:
Gaps:
Download/view:

Download options

Very large alignments can often cause problems for the formatting tool above. If you find that downloading or viewing a large alignment is problematic, you can also download a gzip-compressed, Stockholm-format file containing the seed or full alignment for this family.

You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.

The main seed and full alignments are generated using sequences from the UniProt sequence database. However, we also generate alignments using sequences from the NCBI sequence database and the "metaseq" metagenomics dataset.

You can view alignments from these two additional datasets using the form above, or you can download alignments of NCBI or metagenomics sequences, as gzip-compressed files.

Pfam alignments:
Full length sequences

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 HMMER2.

Pfam alignments:

HMM logo

HMM logos is one way of visualising profile HMMs. Logos provide a quick overview of the properties of an HMM in a graphical form. You can see a more detailed description of HMM logos and find out how you can interpret them here. More...

Trees

This page displays the phylogenetic tree for this family. 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 or full alignments.

Note: You can also download the data files for the seed, full, NCBI or metagenomics trees.

Curation and family details

This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.

Curation View help on the curation process

Seed source: Reference [1] and [2].
Previous IDs: death;
Type: Domain
Author: Bateman A, Griffiths-Jones SR
Number in seed: 91
Number in full: 1116
Average length of the domain: 80.50 aa
Average identity of full alignment: 19 %
Average coverage of the sequence by the domain: 3.34 %

HMM information View help on HMM parameters

HMM build commands:
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 9421015 -E 1000 HMM pfamseq
Model details:
Parameter Sequence Domain
Gathering cut-off 20.3 20.3
Trusted cut-off 20.3 20.3
Noise cut-off 20.2 20.2
Model length: 83
Family (HMM) version: 15
Download: download the raw HMM for this family

Species distribution

Tree controls

Hide

The tree shows the occurrence of this domain across different species. More...

Loading...

Interactions

There are 2 interactions for this family. More...

Death DED

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 MSD 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 Death domain has been found.

Loading structure mapping...