10  structures 122  species 2  interactions 802  sequences 75  architectures

Family: DEP (PF00610)

Summary

Domain found in Dishevelled, Egl-10, and Pleckstrin (DEP) Add an annotation

The DEP domain [1] is responsible for mediating intracellular protein targeting and regulation of protein stability in the cell [2-3]. The DEP domain is present in a number of signaling molecules, including Regulator of G protein Signaling (RGS) proteins, and has been implicated in membrane targeting [4-5]. New findings in yeast, however, demonstrate a major role for a DEP domain in mediating the interaction of an RGS protein to the C-terminal tail of a GPCR, thus placing RGS in close proximity with its substrate G protein alpha subunit [6-7].


Literature references

  1. Ponting CP, Bork P , Trends Biochem Sci 1996;21:245-246.: Pleckstrin's repeat performance: a novel domain in G-protein signaling? PUBMED:8755244

  2. Martemyanov KA, Lishko PV, Calero N, Keresztes G, Sokolov M, Strissel KJ, Leskov IB, Hopp JA, Kolesnikov AV, Chen CK, Lem J, Heller S, Burns ME, Arshavsky VY; , J Neurosci 2003;23:10175-10181.: The DEP domain determines subcellular targeting of the GTPase activating protein RGS9 in vivo. PUBMED:14614075

  3. Keresztes G, Martemyanov KA, Krispel CM, Mutai H, Yoo PJ, Maison SF, Burns ME, Arshavsky VY, Heller S; , J Biol Chem 2004;279:1581-1584.: Absence of the RGS9.Gbeta5 GTPase-activating complex in photoreceptors of the R9AP knockout mouse. PUBMED:14625292

  4. Pan WJ, Pang SZ, Huang T, Guo HY, Wu D, Li L; , Cell Res. 2004;14:324-330.: Characterization of function of three domains in dishevelled-1: DEP domain is responsible for membrane translocation of dishevelled-1. PUBMED:15353129

  5. Kovoor A, Seyffarth P, Ebert J, Barghshoon S, Chen CK, Schwarz S, Axelrod JD, Cheyette BN, Simon MI, Lester HA, Schwarz J; , J Neurosci. 2005;25:2157-2165.: D2 dopamine receptors colocalize regulator of G-protein signaling 9-2 (RGS9-2) via the RGS9 DEP domain, and RGS9 knock-out mice develop dyskinesias associated with dopamine pathways. PUBMED:15728856

  6. Ballon DR, Flanary PL, Gladue DP, Konopka JB, Dohlman HG, Thorner J; , Cell. 2006;126:1079-1093.: DEP-domain-mediated regulation of GPCR signaling responses. PUBMED:16990133

  7. Chen S, Hamm HE; , Dev Cell. 2006;11:436-438.: DEP domains: More than just membrane anchors. PUBMED:17011483


InterPro entry IPR000591

This is a domain of unknown function present in signalling proteins including dishevelled, Egl-10, and pleckstrin proteins. Segment polarity dishevelled protein is required to establish coherent arrays of polarized cells and segments in embryos, and plays a role in wingless signalling. Egl-10 regulates G-protein signalling in the central nervous system. Mammalian regulators of G-protein signalling also contain these domains, and regulate signal transduction by increasing the GTPase activity of G-protein alpha subunits, thereby driving them into their inactive GDP-bound form.

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...

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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...

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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:

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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.

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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: SMART
Previous IDs: none
Type: Domain
Author: Ponting C, Schultz J, Bork P, Martemyanov K, Thorner J
Number in seed: 137
Number in full: 802
Average length of the domain: 72.00 aa
Average identity of full alignment: 24 %
Average coverage of the sequence by the domain: 8.71 %

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 21.2 21.2
Trusted cut-off 21.3 21.2
Noise cut-off 21.1 21.1
Model length: 74
Family (HMM) version: 14
Download: download the raw HMM for this family

Species distribution

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Interactions

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

RasGEF WD40

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 DEP domain has been found.

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