Summary
Proliferating cell nuclear antigen, C-terminal domain
N-terminal and C-terminal domains of PCNA are topologically identical. Three PCNA molecules are tightly associated to form a closed ring encircling duplex DNA.
Literature references
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Krishna TS, Kong XP, Gary S, Burgers PM, Kuriyan J; , Cell 1994;79:1233-1243.: Crystal structure of the eukaryotic DNA polymerase processivity factor PCNA. PUBMED:8001157
InterPro entry IPR000730
Proliferating cell nuclear antigen (PCNA), or cyclin, is a non-histone acidic nuclear protein PUBMED:2884104 that plays a key role in the control of eukaryotic DNA replication PUBMED:1346518. It acts as a co-factor for DNA polymerase delta, which is responsible for leading strand DNA replication PUBMED:2565339. The sequence of PCNA is well conserved between plants and animals, indicating a strong selective pressure for structure conservation, and suggesting that this type of DNA replication mechanism is conserved throughout eukaryotes PUBMED:1671766. In Saccharomyces cerevisiae (Baker's yeast), POL30, is associated with polymerase III, the yeast analog of polymerase delta.
Homologues of PCNA have also been identified in the archaea (Euryarchaeota and Crenarchaeota) and in Paramecium bursaria Chlorella virus 1 (PBCV-1) and in nuclear polyhedrosis viruses.
Clan
This family is a member of clan DNA_clamp (CL0060), which contains the following 10 members:
DNA_pol3_beta DNA_pol3_beta_2 DNA_pol3_beta_3 DNA_PPF Herpes_UL42 Hus1 PCNA_C PCNA_N Rad1 Rad9Gene Ontology
| Cellular component | PCNA complex (GO:0043626) |
| Molecular function | DNA binding (GO:0003677) |
| DNA polymerase processivity factor activity (GO:0030337) | |
| Biological process | regulation of DNA replication (GO:0006275) |
Internal database links
| SCOOP: | Rad1 Hus1 |
External database links
| PANDIT: | PF02747 |
| PROSITE: | PDOC00265 |
| SCOP: | 1plq |
| SYSTERS: | PCNA_C |
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...
View options
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_598 (release 2.1) |
| Previous IDs: | none |
| Type: | Domain |
| Author: | Bateman A, Griffiths-Jones SR |
| Number in seed: | 12 |
| Number in full: | 446 |
| Average length of the domain: | 116.50 aa |
| Average identity of full alignment: | 35 % |
| Average coverage of the sequence by the domain: | 45.67 % |
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: | 128 | ||||||||||||
| Family (HMM) version: | 8 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
Tree controls
HideThe tree shows the occurrence of this domain across different species. More...
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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 PCNA_C domain has been found.
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