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61  structures 3114  species 1  interaction 16073  sequences 69  architectures

Family: Aminotran_5 (PF00266)

Summary: Aminotransferase class-V

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This is the Wikipedia entry entitled "Aminotransferase, class V". More...

Aminotransferase, class V Edit Wikipedia article

Aminotransferase class-V
Identifiers
Symbol Aminotran_5
Pfam PF00266
InterPro IPR000192
PROSITE PDOC00514
SCOP 1bjo
SUPERFAMILY 1bjo

Aminotransferase class-V is an evolutionary conserved protein domain. This domain is found in amino transferases, and other enzymes including cysteine desulphurase EC:4.4.1.-.

Aminotransferases share certain mechanistic features with other pyridoxal- phosphate dependent enzymes, such as the covalent binding of the pyridoxal- phosphate group to a lysine residue. On the basis of sequence similarity, these various enzymes can be grouped[1] into subfamilies. This family is called class-V.

[edit] Subfamilies

[edit] Human proteins containing this domain

AGXT; KYNU; MOCOS; NFS1; PSAT1; SCLY; TLH6;

[edit] References

  1. ^ Sander C, Ouzounis C (1993). "Homology of the NifS family of proteins to a new class of pyridoxal phosphate-dependent enzymes". FEBS Lett. 322 (2): 159–164. doi:10.1016/0014-5793(93)81559-I. PMID 8482384. 


This article incorporates text from the public domain Pfam and InterPro IPR000192

This page is based on a Wikipedia article. The text is available under the Creative Commons Attribution/Share-Alike License.

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.

Aminotransferase class-V

This domain is found in amino transferases, and other enzymes including cysteine desulphurase EC:4.4.1.-.


Clan

This family is a member of clan PLP_aminotran (CL0061), which has a total of 15 members.

Internal database links

External database links

This tab holds annotation information from the InterPro database.

InterPro entry IPR000192

Aminotransferases share certain mechanistic features with other pyridoxal- phosphate dependent enzymes, such as the covalent binding of the pyridoxal- phosphate group to a lysine residue. On the basis of sequence similarity, these various enzymes can be grouped [PUBMED:8482384] into subfamilies. This entry represents the class V aminotransferases and the related, though functionally distinct, cysteine desulfurases.

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...

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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 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: aminotran_5;
Type: Domain
Author: Finn RD
Number in seed: 45
Number in full: 16073
Average length of the domain: 337.90 aa
Average identity of full alignment: 19 %
Average coverage of the sequence by the domain: 83.42 %

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 20.0 20.0
Trusted cut-off 20.0 20.0
Noise cut-off 19.9 19.9
Model length: 371
Family (HMM) version: 14
Download: download the raw HMM for this family

Species distribution

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Interactions

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

Aminotran_5

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 Aminotran_5 domain has been found. There are 61 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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