6  structures 837  species 1  interaction 8444  sequences 26  architectures

Family: Transposase_11 (PF01609)

Summary

Transposase DDE domain Add an annotation

Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction [3]. This family contains transposases for IS4 P03835 [1] IS421 P11901 [2] IS5377 Q45620 IS427 [4] IS402 [5] IS1355 O69604 IS5, which was original isolated in bacteriophage lambda [6].


Literature references

  1. Klaer R, Kuhn S, Tillmann E, Fritz HJ, Starlinger P; , Mol Gen Genet 1981;181:169-175.: The sequence of IS4. PUBMED:6268937

  2. Sato S, Nakada Y, Shiratsuchi A; , FEBS Lett 1989;249:21-26.: IS421, a new insertion sequence in Escherichia coli. PUBMED:2542093

  3. DasSarma S; , Plasmid 1993;29:1-9.: Identification and analysis of the gas vesicle gene cluster on an unstable plasmid of Halobacterium halobium. PUBMED:8335077

  4. Davies DR, Braam LM, Reznikoff WS, Rayment I; , J Biol Chem 1999;274:11904-11913.: The three-dimensional structure of a Tn5 transposase-related protein determined to 2.9-A resolution. PUBMED:10207011

  5. De Meirsman C, Van Soom C, Verreth C, Van Gool A, Vanderleyden J; , Plasmid 1990;24:227-234.: Nucleotide sequence analysis of IS427 and its target sites in Agrobacterium tumefaciens T37. PUBMED:1963949

  6. Ferrante AA, Lessie TG; , Gene 1991;102:143-144.: Nucleotide sequence of IS402 from Pseudomonas cepacia. PUBMED:1650732

  7. Kroger M, Hobom G; , Nature 1982;297:159-162.: Structural analysis of insertion sequence IS5. PUBMED:6281654


InterPro entry IPR002559

Autonomous mobile genetic elements such as transposon or insertion sequences (IS) encode an enzyme, transposase, that is required for excising and inserting the mobile element. Transposases have been grouped into various families PUBMED:8041625, PUBMED:1310791, PUBMED:1718819. This family includes the IS4 transposase.

More information about these proteins can be found at Protein of the Month: Transposase PUBMED:.

Clan

This family is a member of clan RNase_H (CL0219), which contains the following 25 members:

3_5_exonuc CAF1 DDE DNA_pol_B_exo DUF458 Exon_PolB Exonuc_X-T Mu_transposase MULE Phage_Lacto_M3 Piwi Plant_tran Pox_A22 RNase_HII RnaseH RuvC rve Transposase_11 Transposase_12 Transposase_25 Transposase_27 Transposase_29 Transposase_mut UPF0236 Ydc2-catalyt

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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Alignment:
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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_1013 (release 4.1)
Previous IDs: none
Type: Domain
Author: Bateman A
Number in seed: 92
Number in full: 8444
Average length of the domain: 189.40 aa
Average identity of full alignment: 12 %
Average coverage of the sequence by the domain: 59.89 %

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 23.0 23.0
Trusted cut-off 23.0 23.0
Noise cut-off 22.9 22.9
Model length: 207
Family (HMM) version: 14
Download: download the raw HMM for this family

Species distribution

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

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Interactions

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

Transposase_Tn5

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 Transposase_11 domain has been found.

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