Summary: Amelogenin
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Amelogenin Provide feedback
Amelogenins play a role in biomineralisation. They seem to regulate the formation of crystallites during the secretory stage of tooth enamel development. thought to play a major role in the structural organisation and mineralisation of developing enamel. They are found in the extracellular matrix. Mutations in X-chromosomal amelogenin can cause Amelogenesis imperfecta [1].
Literature references
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Li W, Gibson CW, Abrams WR, Andrews DW, DenBesten PK; , Matrix Biol 2001;19:755-760.: Reduced hydrolysis of amelogenin may result in X-linked amelogenesis imperfecta. PUBMED:11223334 EPMC:11223334
External database links
| PANDIT: | PF02948 |
| Pseudofam: | PF02948 |
| SYSTERS: | Amelogenin |
This tab holds annotation information from the InterPro database.
InterPro entry IPR004116
Amelogenins, cell adhesion proteins, play a role in the biomineralisation of teeth. They seem to regulate formation of crystallites during the secretory stage of tooth enamel development and are thought to play a major role in the structural organisation and mineralisation of developing enamel. The extracellular matrix of the developing enamel comprises two major classes of protein: the hydrophobic amelogenins and the acidic enamelins [PUBMED:8118759].
Circular dichroism studies of porcine amelogenin have shown that the protein consists of 3 discrete folding units [PUBMED:8454575]: the N-terminal region appears to contain beta-strand structures, while the C-terminal region displays characteristics of a random coil conformation. Subsequent studies on the bovine protein have indicated the amelogenin structure to contain a repetitive beta-turn segment and a "beta-spiral" between Gln112 and Leu138, which sequester a (Pro, Leu, Gln) rich region [PUBMED:2598664]. The beta-spiral offers a probable site for interactions with Ca2+ ions.
Muatations in the human amelogenin gene (AMGX) cause X-linked hypoplastic amelogenesis imperfecta, a disease characterised by defective enamel. A 9bp deletion in exon 2 of AMGX results in the loss of codons for Ile5, Leu6, Phe7 and Ala8, and replacement by a new threonine codon, disrupting the 16-residue (Met1-Ala16) amelogenin signal peptide [PUBMED:7782077].
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Cellular component | proteinaceous extracellular matrix (GO:0005578) |
| Biological process | multicellular organismal development (GO:0007275) |
Domain organisation
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Alignments
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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 (6) |
Full (451) |
Representative proteomes | NCBI (407) |
Meta (0) |
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| RP15 (2) |
RP35 (2) |
RP55 (6) |
RP75 (28) |
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| PP/heatmap | 1 | |||||||
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1Cannot generate PP/Heatmap alignments for seeds; no PP data available
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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 (6) |
Full (451) |
Representative proteomes | NCBI (407) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (2) |
RP35 (2) |
RP55 (6) |
RP75 (28) |
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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_402 (release 6.4) |
| Previous IDs: | none |
| Type: | Family |
| Author: | Bateman A |
| Number in seed: | 6 |
| Number in full: | 451 |
| Average length of the domain: | 113.20 aa |
| Average identity of full alignment: | 52 % |
| Average coverage of the sequence by the domain: | 97.18 % |
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: | 174 | ||||||||||||
| Family (HMM) version: | 10 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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