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0  structures 35  species 0  interactions 37  sequences 1  architecture

Family: CRPA (PF05745)

Summary: Chlamydia 15 kDa cysteine-rich outer membrane protein (CRPA)

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Chlamydia 15 kDa cysteine-rich outer membrane protein (CRPA) Provide feedback

This family consists of several Chlamydia 15 kDa cysteine-rich outer membrane proteins which are associated with differentiation of reticulate bodies (RBs) into elementary bodies (EBs) [1].

Literature references

  1. Clarke IN, Ward ME, Lambden PR; , Gene 1988;71:307-314.: Molecular cloning and sequence analysis of a developmentally regulated cysteine-rich outer membrane protein from Chlamydia trachomatis. PUBMED:3066701 EPMC:3066701

  2. de la Maza LM, Fielder TJ, Carlson EJ, Markoff BA, Peterson EM; , Infect Immun 1991;59:1196-1201.: Sequence diversity of the 60-kilodalton protein and of a putative 15-kilodalton protein between the trachoma and lymphogranuloma venereum biovars of Chlamydia trachomatis. PUBMED:1997423 EPMC:1997423


External database links

This tab holds annotation information from the InterPro database.

InterPro entry IPR008436

Chlamydia is a genus of bacteria, which causes the most common bacterial sexually transmitted diseases. They are obligate intracellular bacterial pathogens. Members of this genus lack a peptidoglycan layer, but as a substitute, it has been proposed that they have several cysteine rich membrane proteins. This includes the major outer membrane protein (MOMP). These form disulphide bonds to provide rigidity to the cell wall. The alignment of the amino acid sequences of the MOMP from various serovars of Chlamydia show that they have between seven and ten cysteine residues; seven of which are highly conserved [PUBMED:15835913]. The MOMP has been the focus of efforts to produce a vaccine for Chlamydia trachomatis [PUBMED:17601785]. The 15 kDa cysteine-rich protein in this entry is a multi-pass outer membrane protein. They are associated with the differentiation of reticulate bodies (RBs) into elementary bodies (EBs) [PUBMED:3066701]. They immunolocalise to the inclusion membrane, which is the membrane that surrounds the intracellular parasite. These proteins are recognised by CD8+ T cells in both human and mouse infections, suggesting they gain access to the host cytoplasm.

Gene Ontology

The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.

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
(5)
Full
(37)
Representative proteomes NCBI
(18)
Meta
(0)
RP15
(1)
RP35
(1)
RP55
(3)
RP75
(4)
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1Cannot generate PP/Heatmap alignments for seeds; no PP data available

Key: ✓ available, x not generated, not available.

Format an alignment

  Seed
(5)
Full
(37)
Representative proteomes NCBI
(18)
Meta
(0)
RP15
(1)
RP35
(1)
RP55
(3)
RP75
(4)
Alignment:
Format:
Order:
Sequence:
Gaps:
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Download options

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
(5)
Full
(37)
Representative proteomes NCBI
(18)
Meta
(0)
RP15
(1)
RP35
(1)
RP55
(3)
RP75
(4)
Raw Stockholm Download   Download   Download   Download   Download   Download   Download    
Gzipped Download   Download   Download   Download   Download   Download   Download    

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.

Pfam alignments:

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 View help on the curation process

Seed source: Pfam-B_6389 (release 8.0)
Previous IDs: none
Type: Family
Author: Moxon SJ
Number in seed: 5
Number in full: 37
Average length of the domain: 131.10 aa
Average identity of full alignment: 62 %
Average coverage of the sequence by the domain: 84.93 %

HMM information View help on HMM parameters

HMM build commands:
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
Model details:
Parameter Sequence Domain
Gathering cut-off 23.6 23.6
Trusted cut-off 144.2 143.9
Noise cut-off 23.5 23.5
Model length: 150
Family (HMM) version: 6
Download: download the raw HMM for this family

Species distribution

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