Summary
Porphyromonas gingivalis major fimbrial subunit protein (FimA)
This family consists of several Porphyromonas gingivalis major fimbrial subunit protein (FimA) sequences. Fimbriae of Porphyromonas gingivalis, a periodontopathogen, play an important role in its adhesion to and invasion of host cells. The fimA genes encoding fimbrillin (FimA), a subunit protein of fimbriae, have been classified into five types, types I to V, based on nucleotide sequences. It has been found that type II FimA can bind to epithelial cells most efficiently through specific host receptors [1].
Literature references
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Nakagawa I, Amano A, Kuboniwa M, Nakamura T, Kawabata S, Hamada S; , Infect Immun 2002;70:277-285.: Functional differences among FimA variants of Porphyromonas gingivalis and their effects on adhesion to and invasion of human epithelial cells. PUBMED:11748193
InterPro entry IPR008110
Periodontal disease in humans is a major health problem in the developed world, and is caused by a number of specialised pathogens that inhabit the oral cavity. Amongst the bacterial species culturable from periodontal lesions are the streptococcal microbes Streptococcus mutans and Streptococcus sobrinus, and the Gram-negative anaerobe Porphyromonas gingivalis (Bacteroides gingivalis) PUBMED:2895100. The latter bacterium has been implicated as the causative agent of peridontitis, pulpal infections and tonsillar abcesses PUBMED:2895100.
Adherence by P. gingivalis to the periodontal surface is mediated by its major virulence factor fimbriae PUBMED:1987052. This differs from other pathogenic Gram-negative bacterial polymeric Type I and IV fimbriae/pili in that it is much more simplified, consisting of only a monomeric fimbrillin repeating subunit, Fma1/FimA. Fma1/FimA has a molecular weight of 43kDa, and can exhibit antigenic diversity in different P. gingivalis strains PUBMED:1987052. Unusually, this form of fimbrillin possesses a far longer leader peptide compared to the fimbrial subunits of other bacteria PUBMED:1987052. It has been hypothesised that this allows for the maturation of the preprotein during secretion PUBMED:1987052.
Recently, a study into the different antigenic types of P. gingivalis fimbrillin classified them into five distinct groups, depending on their gene sequences PUBMED:11748193. Investigations into the functional differences of each type revealed that in the majority of peridontitis cases, bacterial strains possessing the type II Fma1/FimA were the most prevalent PUBMED:11748193; in healthy adults, type I strains were the most common. This has implications for particular strains that are associated with periodontal disease.
Gene Ontology
| Molecular function | structural molecule activity (GO:0005198) |
External database links
| PANDIT: | PF06321 |
| SYSTERS: | P_gingi_FimA |
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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Formatting options
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.
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.
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
| Seed source: | Pfam-B_13339 (release 9.0) |
| Previous IDs: | none |
| Type: | Family |
| Author: | Moxon SJ |
| Number in seed: | 4 |
| Number in full: | 40 |
| Average length of the domain: | 283.20 aa |
| Average identity of full alignment: | 35 % |
| Average coverage of the sequence by the domain: | 68.25 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 9421015 -E 1000 HMM pfamseq
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| Model details: |
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| Model length: | 347 | ||||||||||||
| Family (HMM) version: | 4 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
Tree controls
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