Summary: PDE8 phosphodiesterase
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PDE8 phosphodiesterase Provide feedback
This region is found in members of the PDE8 phosphodiesterase family [1]. It is found with PF00233.
Literature references
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Hayashi M, Matsushima K, Ohashi H, Tsunoda H, Murase S, Kawarada Y, Tanaka T; , Biochem Biophys Res Commun. 1998;250:751-756.: Molecular cloning and characterization of human PDE8B, a novel thyroid-specific isozyme of 3',5'-cyclic nucleotide phosphodiesterase. PUBMED:9784418 EPMC:9784418
External database links
| PANDIT: | PF08629 |
| Pseudofam: | PF08629 |
| SYSTERS: | PDE8 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR013938
The cyclic nucleotide phosphodiesterases (PDE) comprise a group of enzymes that degrade the phosphodiester bond in the second messenger molecules cAMP and cGMP. They are divided into 11 families. They regulate the localisation, duration and amplitude of cyclic nucleotide signalling within subcellular domains. PDEs are therefore important for signal transduction.
PDE enzymes are often targets for pharmacological inhibition due to their unique tissue distribution, structural properties, and functional properties. Inhibitors include: Roflumilast for chronic obstructive pulmonary disease and asthma [PUBMED:18447606], Sildenafil for erectile dysfunction [PUBMED:18367027] and Cilostazol for peripheral arterial occlusive disease [PUBMED:18436153], amongst others.
Retinal 3',5'-cGMP phosphodiesterase is located in photoreceptor outer segments: it is light activated, playing a pivotal role in signal transduction. In rod cells, PDE is oligomeric, comprising an alpha-, a beta- and 2 gamma-subunits, while in cones, PDE is a homodimer of alpha chains, which are associated with several smaller subunits. Both rod and cone PDEs catalyse the hydrolysis of cAMP or cGMP to the corresponding nucleoside 5' monophosphates, both enzymes also binding cGMP with high affinity. The cGMP-binding sites are located in the N-terminal half of the protein sequence, while the catalytic core resides in the C-terminal portion.
This region is found at the N terminus of members of PDE8 phosphodiesterase family [PUBMED:9784418]. Phosphodiesterase 8 (PDE8) regulates chemotaxis of activated lymphocytes [PUBMED:16696947].
Domain organisation
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Alignments
We store a range of different sequence alignments for families. As well as the seed alignment from which the family is built, we provide the full alignment, generated by searching the sequence database using the family HMM. We also generate alignments using four representative proteomes (RP) sets, the NCBI sequence database, and our metagenomics sequence database. More...
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We make a range of alignments for each Pfam-A family. You can see a description of each above. You can view these alignments in various ways but please note that some types of alignment are never generated while others may not be available for all families, most commonly because the alignments are too large to handle.
| Seed (2) |
Full (24) |
Representative proteomes | NCBI (46) |
Meta (0) |
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| RP15 (3) |
RP35 (4) |
RP55 (7) |
RP75 (8) |
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| PP/heatmap | 1 | |||||||
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1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
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not generated,
— not available.
Format an alignment
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We make all of our alignments available in Stockholm format. You can download them here as raw, plain text files or as gzip-compressed files.
| Seed (2) |
Full (24) |
Representative proteomes | NCBI (46) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (3) |
RP35 (4) |
RP55 (7) |
RP75 (8) |
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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
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'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.
Note: You can also download the data file for the tree.
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
| Seed source: | Pfam-B_72889 (release 17.0) |
| Previous IDs: | none |
| Type: | Family |
| Author: | Mistry J, Vasta V |
| Number in seed: | 2 |
| Number in full: | 24 |
| Average length of the domain: | 49.50 aa |
| Average identity of full alignment: | 77 % |
| Average coverage of the sequence by the domain: | 6.74 % |
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: | 52 | ||||||||||||
| Family (HMM) version: | 5 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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