Please note: this site relies heavily on the use of javascript. Without a javascript-enabled browser, this site will not function correctly. Please enable javascript and reload the page, or switch to a different browser.
133  structures 2842  species 2  interactions 8886  sequences 121  architectures

Family: Pro_isomerase (PF00160)

Summary: Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD

Pfam includes annotations and additional family information from a range of different sources. These sources can be accessed via the tabs below.

The Pfam group coordinates the annotation of Pfam families in Wikipedia, but we have not yet assigned a Wikipedia article to this family. If you think that a particular Wikipedia article provides good annotation, please let us know.

This tab holds the annotation information that is stored in the Pfam database. As we move to using Wikipedia as our main source of annotation, the contents of this tab will be gradually replaced by the Wikipedia tab.

Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD Add an annotation

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

  1. Wang P, Heitman J; , Genome Biol 2005;6:226.: The cyclophilins. PUBMED:15998457



Clan

This family is a member of clan Cyclophil-like (CL0475), which has a total of 6 members.

External database links

This tab holds annotation information from the InterPro database.

InterPro entry IPR002130

Cyclophilin [PUBMED:14731520] is the major high-affinity binding protein in vertebrates for the immunosuppressive drug cyclosporin A (CSA), but is also found in other organisms. It exhibits a peptidyl-prolyl cis-trans isomerase activity (EC) (PPIase or rotamase). PPIase is an enzyme that accelerates protein folding by catalysing the cis-trans isomerisation of proline imidic peptide bonds in oligopeptides [PUBMED:2186809]. It is probable that CSA mediates some of its effects via an forming a tight complex with cyclophilin that inhibits the phosphatase activity of calcineurin [PUBMED:7514602], [PUBMED:8117697]. Cyclophilin A is a cytosolic and highly abundant protein. The protein belongs to a family of isozymes, including cyclophilins B and C, and natural killer cell cyclophilin-related protein [PUBMED:1464374, PUBMED:8404888, PUBMED:7526121]. Major isoforms have been found throughout the cell, including the ER, and some are even secreted. The sequences of the different forms of cyclophilin-type PPIases are well conserved.

  • Note: FKBP's, a family of proteins that bind the immunosuppressive drug FK506, are also PPIases, but their sequence is not at all related to that of cyclophilin (see INTERPRO).
  • Gene Ontology

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

    Domain organisation

    Below is a listing of the unique domain organisations or architectures in which this domain is found. More...

    Loading domain graphics...

    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_isomerase

    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...

    View options

    Alignment:
    Viewer:  

    Formatting options

    Alignment:
    Format:
    Order:
    Sequence:
    Gaps:
    Download/view:

    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.

    Pfam alignments:
    Full length sequences

    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. 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 View help on the curation process

    Seed source: Prosite
    Previous IDs: pro_isomerase;
    Type: Domain
    Author: Sonnhammer ELL, Wuster A
    Number in seed: 169
    Number in full: 8886
    Average length of the domain: 159.40 aa
    Average identity of full alignment: 34 %
    Average coverage of the sequence by the domain: 62.11 %

    HMM information View help on HMM parameters

    HMM build commands:
    build method: hmmbuild -o /dev/null HMM SEED
    search method: hmmsearch -Z 15929002 -E 1000 --cpu 4 HMM pfamseq
    Model details:
    Parameter Sequence Domain
    Gathering cut-off 20.8 20.8
    Trusted cut-off 20.8 20.8
    Noise cut-off 20.5 20.6
    Model length: 155
    Family (HMM) version: 16
    Download: download the raw HMM for this family

    Species distribution

    Sunburst controls

    Hide

    Weight segments by...


    Change the size of the sunburst

    Small
    Large

    Colour assignments

    Archea Archea Eukaryota Eukaryota
    Bacteria Bacteria Other sequences Other sequences
    Viruses Viruses Unclassified Unclassified
    Viroids Viroids Unclassified sequence Unclassified sequence

    This visualisation provides a simple graphical representation of the distribution of this family across species. You can find the original interactive tree in the adjacent tab if you need to select sub-trees and view sequence alignments. More...

    Tree controls

    Hide

    The tree shows the occurrence of this domain across different species. More...

    Loading...

    Please note: for large trees this can take some time. While the tree is loading, you can safely switch away from this tab but if you browse away from the family page entirely, the tree will not be loaded.

    Interactions

    There are 2 interactions for this family. More...

    Pro_isomerase PRP4

    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 133 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.

    Loading structure mapping...