Summary: Function to find
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Function to find Provide feedback
The function to find (FIIND) was initially discovered in two proteins, NLRP1 (aka NALP1, CARD7, NAC, DEFCAP) and CARD8 (aka TUCAN, Cardinal) [1]. NLRP1 is a member of the Nod-like receptor (NLR) protein superfamily and is involved in apoptosis and inflammation. To date, it is the only NLR protein known to have a FIIND domain. The FIIND domain is also present in the CARD8 protein where, like in NLRP1, it is followed by a C-terminal CARD domain. Both proteins are described to form an "inflammasome", a macro-molecular complex able to process caspase 1 and activate pro-IL1beta [2]. The FIIND domain is present in only a very small subset of the kingdom of life, comprising primates, rodents (mouse, rat), carnivores (dog) and a few more, such as horse. The function of this domain is yet to be determined. Publications describing the newly discovered NLRP1 protein failed to identify it as a separate domain; for example, it was taken as part of the adjacent leucine rich repeat domain (LRR) [3]. Upon discovery of CARD8 it was noted that the N-terminal region shared significant sequence identity with an undescribed region in NLRP1 [1]. Before getting its final name, FIIND [4] this domain was termed NALP1-associated domain (NAD) [5].
Literature references
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Pathan N, Marusawa H, Krajewska M, Matsuzawa S, Kim H, Okada K, Torii S, Kitada S, Krajewski S, Welsh K, Pio F, Godzik A, Reed JC;, J Biol Chem. 2001;276:32220-32229.: TUCAN, an antiapoptotic caspase-associated recruitment domain family protein overexpressed in cancer. PUBMED:11408476 EPMC:11408476
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Tschopp J, Martinon F, Burns K;, Nat Rev Mol Cell Biol. 2003;4:95-104.: NALPs: a novel protein family involved in inflammation. PUBMED:12563287 EPMC:12563287
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Hlaing T, Guo RF, Dilley KA, Loussia JM, Morrish TA, Shi MM, Vincenz C, Ward PA;, J Biol Chem. 2001;276:9230-9238.: Molecular cloning and characterization of DEFCAP-L and -S, two isoforms of a novel member of the mammalian Ced-4 family of apoptosis proteins. PUBMED:11076957 EPMC:11076957
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Tschopp J, Martinon F, Burns K;, Nat Rev Mol Cell Biol. 2003;4:95-104.: NALPs: a novel protein family involved in inflammation. PUBMED:12563287 EPMC:12563287
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Martinon F, Burns K, and Tschopp J, Mol Cell. 2002;10:417-26.: The Inflammasome: A Molecular Platform Triggering Activation of Inflammatory Caspases and Processing of proIL-beta. PUBMED:12191486 EPMC:12191486
External database links
| PANDIT: | PF13553 |
| Pseudofam: | PF13553 |
| SYSTERS: | FIIND |
This tab holds annotation information from the InterPro database.
InterPro entry IPR025307
The function to find (FIIND) domain was initially discovered in two proteins, NLRP1 (aka NALP1, CARD7, NAC, DEFCAP) and CARD8 (aka TUCAN, Cardinal) [PUBMED:11408476]. NLRP1 is a member of the Nod-like receptor (NLR) protein superfamily and is involved in apoptosis and inflammation. To date, it is the only NLR protein known to have a FIIND domain. The FIIND domain is also present in the CARD8 protein where, like in NLRP1, it is followed by a C-terminal CARD domain. Both proteins are described to form an "inflammasome", a macro-molecular complex able to process caspase 1 and activate pro-IL1beta [PUBMED:12563287]. The FIIND domain is present in only a very small subset of the kingdom of life, comprising primates, rodents (mouse, rat), carnivores (dog) and a few more, such as horse. The function of this domain is yet to be determined. Publications describing the newly discovered NLRP1 protein failed to identify it as a separate domain; for example, it was taken as part of the adjacent leucine rich repeat domain (LRR) [PUBMED:11076957]. Upon discovery of CARD8 it was noted that the N-terminal region shared significant sequence identity with an undescribed region in NLRP1 [PUBMED:11408476]. Before getting its final name, FIIND [PUBMED:12563287], this domain was termed NALP1-associated domain (NAD) [PUBMED:12191486].
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
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 (7) |
Full (140) |
Representative proteomes | NCBI (160) |
Meta (0) |
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| RP15 (20) |
RP35 (29) |
RP55 (43) |
RP75 (69) |
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| Jalview | ||||||||
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| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
available,
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 (7) |
Full (140) |
Representative proteomes | NCBI (160) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (20) |
RP35 (29) |
RP55 (43) |
RP75 (69) |
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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: | Joint Center of Structural Genomics (JCSG) |
| Previous IDs: | none |
| Type: | Family |
| Author: | Weichenberger CX, D'Osualdo A |
| Number in seed: | 7 |
| Number in full: | 140 |
| Average length of the domain: | 224.30 aa |
| Average identity of full alignment: | 41 % |
| Average coverage of the sequence by the domain: | 24.92 % |
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: | 255 | ||||||||||||
| Family (HMM) version: | 1 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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