Summary: Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD
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Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD Provide feedback
The peptidyl-prolyl cis-trans isomerases, also known as cyclophilins, share this domain of about 109 amino acids. Cyclophilins have been found in all organisms studied so far and catalyse peptidyl-prolyl isomerisation during which the peptide bond preceding proline (the peptidyl-prolyl bond) is stabilised in the cis conformation. Mammalian cyclophilin A (CypA) is a major cellular target for the immunosuppressive drug cyclosporin A (CsA). Other roles for cyclophilins may include chaperone and cell signalling function [1].
Literature references
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Wang P, Heitman J; , Genome Biol 2005;6:226.: The cyclophilins. PUBMED:15998457 EPMC:15998457
External database links
| HOMSTRAD: | cyclo |
| PANDIT: | PF00160 |
| PRINTS: | PR00153 |
| PROSITE: | PDOC00154 |
| Pseudofam: | PF00160 |
| SCOP: | 1cyh |
| SYSTERS: | Pro_isomerase |
This tab holds annotation information from the InterPro database.
InterPro entry IPR002130
Cyclophilins exhibit peptidyl-prolyl cis-trans isomerase (PPIase) activity (EC), accelerating protein folding by catalysing the cis-trans isomerisation of proline imidic peptide bonds in oligopeptides [PUBMED:14731520, PUBMED:2186809]. They also have protein chaperone-like functions [PUBMED:15998457] and are the major high-affinity binding proteins for the immunosuppressive drug cyclosporin A (CSA) in vertebrates [PUBMED:14731520].
Cyclophilins are found in all prokaryotes and eukaryotes, and have been structurally conserved throughout evolution, implying their importance in cellular function [PUBMED:21309470]. They share a common 109 amino acid cyclophilin-like domain (CLD) and additional domains unique to each member of the family. The CLD domain contains the PPIase activity, while the unique domains are important for selection of protein substrates and subcellular compartmentalisation [PUBMED:21295323].
This entry represents the core beta-barrel cyclophilin-like domain.Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
| Molecular function | peptidyl-prolyl cis-trans isomerase activity (GO:0003755) |
| Biological process | protein folding (GO:0006457) |
Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Pfam Clan
This family is a member of clan Cyclophil-like (CL0475), which contains the following 6 members:
AHS1 Cyclophil_like DUF3830 DUF871 PIF Pro_isomeraseAlignments
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...
View options
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 (168) |
Full (13237) |
Representative proteomes | NCBI (10643) |
Meta (4524) |
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| RP15 (1874) |
RP35 (3188) |
RP55 (4422) |
RP75 (5300) |
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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,
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Format an alignment
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 (168) |
Full (13237) |
Representative proteomes | NCBI (10643) |
Meta (4524) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (1874) |
RP35 (3188) |
RP55 (4422) |
RP75 (5300) |
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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: | Prosite |
| Previous IDs: | pro_isomerase; |
| Type: | Domain |
| Author: | Sonnhammer ELL, Wuster A |
| Number in seed: | 168 |
| Number in full: | 13237 |
| Average length of the domain: | 159.30 aa |
| Average identity of full alignment: | 35 % |
| Average coverage of the sequence by the domain: | 60.14 % |
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: | 155 | ||||||||||||
| Family (HMM) version: | 16 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Interactions
Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the Pro_isomerase domain has been found. There are 283 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein seqence.
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Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence