2  structures 164  species 1  interaction 585  sequences 8  architectures

Family: Topo_Zn_Ribbon (PF08272)

Summary

Topoisomerase I zinc-ribbon-like Add an annotation

Some Proteobacteria topoisomerase I contain two zinc-ribbon-like domains at the C-terminus that structurally homologous to PF01396. However, this domain no longer bind zinc. Indeed, only one of the four cysteine residues remains [1].


Literature references

  1. Grishin NV; , J Mol Biol 2000;299:1165-1177.: C-terminal domains of Escherichia coli topoisomerase I belong to the zinc-ribbon superfamily. PUBMED:10873443


InterPro entry IPR013263

DNA topoisomerases regulate the number of topological links between two DNA strands (i.e. change the number of superhelical turns) by catalysing transient single- or double-strand breaks, crossing the strands through one another, then resealing the breaks. These enzymes have several functions: to remove DNA supercoils during transcription and DNA replication; for strand breakage during recombination; for chromosome condensation; and to disentangle intertwined DNA during mitosis PUBMED:12042765, PUBMED:11395412. DNA topoisomerases are divided into two classes: type I enzymes (; topoisomerases I, III and V) break single-strand DNA, and type II enzymes (; topoisomerases II, IV and VI) break double-strand DNA PUBMED:12596227.

Type I topoisomerases are ATP-independent enzymes (except for reverse gyrase), and can be subdivided according to their structure and reaction mechanisms: type IA (bacterial and archaeal topoisomerase I, topoisomerase III and reverse gyrase) and type IB (eukaryotic topoisomerase I and topoisomerase V). These enzymes are primarily responsible for relaxing positively and/or negatively supercoiled DNA, except for reverse gyrase, which can introduce positive supercoils into DNA.

This entry represents the C-terminal zinc-ribbon-like domain found in bacterial topoisomerase I (type IA) enzymes. Escherichia coli topoisomerase I proteins contain five copies of a zinc-ribbon-like domain at their C-terminus, two of which have lost their cysteine residues and are therefore probably not able to bind zinc PUBMED:10873443. This domain is still considered to be a member of the zinc-ribbon superfamily despite not being able to bind zinc.

More information about this protein can be found at Protein of the Month: DNA Topoisomerase PUBMED:.

Clan

This family is a member of clan Zn_Beta_Ribbon (CL0167), which contains the following 30 members:

A2L_zn_ribbon Auto_anti-p27 Baculo_LEF5_C CxxC_CxxC_SSSS DNA_RNApol_7kD DUF1407 DUF1610 DUF1936 DUF2387 Elf1 GATA Ogr_Delta PhnA_Zn_Ribbon Prim_Zn_Ribbon Ribosomal_S27 Ribosomal_S27e RNA_POL_M_15KD RRN7 Spt4 TF_Zn_Ribbon TFIIS_C Topo_Zn_Ribbon Transposase_35 Trm112p UPF0547 zf-C4_Topoisom zf-CHC2 zf-dskA_traR zf-GRF zf-NADH-PPase

Gene Ontology

External database links

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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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 HMMER2.

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: Pfam-B_5615 (release 17.0)
Previous IDs: none
Type: Domain
Author: Finn RD
Number in seed: 19
Number in full: 585
Average length of the domain: 41.40 aa
Average identity of full alignment: 38 %
Average coverage of the sequence by the domain: 4.81 %

HMM information View help on HMM parameters

HMM build commands:
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 9421015 -E 1000 HMM pfamseq
Model details:
Parameter Sequence Domain
Gathering cut-off 25.0 25.0
Trusted cut-off 28.9 28.9
Noise cut-off 17.4 16.4
Model length: 42
Family (HMM) version: 4
Download: download the raw HMM for this family

Species distribution

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Interactions

There is 1 interaction for this family. More...

Topo_Zn_Ribbon

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 MSD 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 Topo_Zn_Ribbon domain has been found.

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