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222  structures 7859  species 0  interactions 34234  sequences 230  architectures

Family: ACT (PF01842)

Summary: ACT domain

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

This is the Wikipedia entry entitled "ACT domain". More...

ACT domain Edit Wikipedia article

ACT
PDB 2j0w EBI.jpg
crystal structure of e. coli aspartokinase iii in complex with aspartate and adp (r-state)
Identifiers
SymbolACT
PfamPF01842
Pfam clanCL0070
InterProIPR002912
SCOP21psd / SCOPe / SUPFAM

In molecular biology, the ACT domain is a protein domain that is found in a variety of contexts and is proposed to be a conserved regulatory binding fold. ACT domains are linked to a wide range of metabolic enzymes that are regulated by amino acid concentration. The archetypical ACT domain is the C-terminal regulatory domain of 3-phosphoglycerate dehydrogenase (3PGDH), which folds with a ferredoxin-like topology. A pair of ACT domains form an eight-stranded antiparallel sheet with two molecules of allosteric inhibitor serine bound in the interface. Biochemical exploration of a few other proteins containing ACT domains supports the suggestions that these domains contain the archetypical ACT structure.[1]

References

  1. ^ Chipman DM, Shaanan B (2001). "The ACT domain family". Curr. Opin. Struct. Biol. 11 (6): 694–700. PMID 11751050. {{cite journal}}: Unknown parameter |month= ignored (help)
This article incorporates text from the public domain Pfam and InterPro: IPR002912

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.

ACT domain Provide feedback

This family of domains generally have a regulatory role. ACT domains are linked to a wide range of metabolic enzymes that are regulated by amino acid concentration. Pairs of ACT domains bind specifically to a particular amino acid leading to regulation of the linked enzyme. The ACT domain is found in: D-3-phosphoglycerate dehydrogenase EC:1.1.1.95 P08328 which is inhibited by serine [1]. Aspartokinase EC:2.7.2.4 P53553 which is regulated by lysine. Acetolactate synthase small regulatory subunit P00894 which is inhibited by valine. Phenylalanine-4-hydroxylase EC:1.14.16.1 P00439 which is regulated by phenylalanine. Prephenate dehydrogenase EC:4.2.1.51 P21203. formyltetrahydrofolate deformylase EC:3.5.1.10, P37051 which is activated by methionine and inhibited by glycine. GTP pyrophosphokinase EC:2.7.6.5 P11585

Literature references

  1. Schuller DJ, Grant GA, Banaszak LJ; , Nat Struct Biol 1995;2:69-76.: The allosteric ligand site in the Vmax-type cooperative enzyme phosphoglycerate dehydrogenase. PUBMED:7719856 EPMC:7719856

  2. Aravind L, Koonin EV; , J Mol Biol 1999;287:1023-1040.: Gleaning non-trivial structural, functional and evolutionary information about proteins by iterative database searches. PUBMED:10222208 EPMC:10222208


Internal database links

External database links

This tab holds annotation information from the InterPro database.

InterPro entry IPR002912

The ACT domain is found in a variety of contexts and is proposed to be a conserved regulatory binding fold. ACT domains are linked to a wide range of metabolic enzymes that are regulated by amino acid concentration. The archetypical ACT domain is the C-terminal regulatory domain of 3-phosphoglycerate dehydrogenase (3PGDH), which folds with a ferredoxin-like topology. A pair of ACT domains form an eight-stranded antiparallel sheet with two molecules of allosteric inhibitor serine bound in the interface. Biochemical exploration of a few other proteins containing ACT domains supports the suggestions that these domains contain the archetypical ACT structure [ PUBMED:11751050 ].

Most of the proteins in which it is found are involved in amino acid and purine metabolism:

  • aspartokinases
  • chorismate mutases
  • prephenate dehydrogenases (TyrA)
  • prephenate dehydratases
  • homoserine dehydrogenases
  • malate dehydrogenases
  • phosphoglycerate dehydrogenases
  • phenylalanine and tryptophan-4-monooxygenases
  • phosphoribosylformylglycinamidine synthase (PurQ)
  • uridylyl transferase and removing enzyme (GlnD)
  • GTP pyrophosphokinase/phosphohydrolase (SpoT/RelA)
  • tyrosine and phenol metabolism operon regulators (TyrR)
  • several uncharacterised proteins from archaea, bacteria and plants that contain from one to four copies of this domain [ PUBMED:12481063 ].

Domain organisation

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

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Pfam Clan

This family is a member of clan ACT (CL0070), which has the following description:

These domains are involved in binding to amino-acids and causing allosteric regulation of linked enzyme domains [1]. The relationship between these two families was first noticed in [2].

The clan contains the following 12 members:

ACT ACT_3 ACT_4 ACT_5 ACT_6 ACT_7 ACT_8 ALS_ss_C DUF493 NikR_C NIL Thr_dehydrat_C

Alignments

We store a range of different sequence alignments for families. As well as the seed alignment from which the family is built, we provide the full alignment, generated by searching the sequence database (reference proteomes) using the family HMM. We also generate alignments using four representative proteomes (RP) sets and the UniProtKB sequence database. More...

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We make a range of alignments for each Pfam-A family. You can see a description of each above. You can view these alignments in various ways but please note that some types of alignment are never generated while others may not be available for all families, most commonly because the alignments are too large to handle.

  Seed
(128)
Full
(34234)
Representative proteomes UniProt
(141309)
RP15
(4361)
RP35
(16787)
RP55
(34262)
RP75
(57214)
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PP/heatmap 1            

1Cannot generate PP/Heatmap alignments for seeds; no PP data available

Key: ✓ available, x not generated, not available.

Format an alignment

  Seed
(128)
Full
(34234)
Representative proteomes UniProt
(141309)
RP15
(4361)
RP35
(16787)
RP55
(34262)
RP75
(57214)
Alignment:
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We make all of our alignments available in Stockholm format. You can download them here as raw, plain text files or as gzip-compressed files.

  Seed
(128)
Full
(34234)
Representative proteomes UniProt
(141309)
RP15
(4361)
RP35
(16787)
RP55
(34262)
RP75
(57214)
Raw Stockholm Download   Download   Download   Download   Download   Download   Download  
Gzipped Download   Download   Download   Download   Download   Download   Download  

You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.

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's seed alignment. 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 alignment.

Note: You can also download the data file for the tree.

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: Bateman A
Previous IDs: none
Type: Domain
Sequence Ontology: SO:0000417
Author: Bateman A
Number in seed: 128
Number in full: 34234
Average length of the domain: 65.2 aa
Average identity of full alignment: 18 %
Average coverage of the sequence by the domain: 17.21 %

HMM information View help on HMM parameters

HMM build commands:
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 61295632 -E 1000 --cpu 4 HMM pfamseq
Model details:
Parameter Sequence Domain
Gathering cut-off 27.0 27.0
Trusted cut-off 27.0 27.0
Noise cut-off 26.9 26.9
Model length: 66
Family (HMM) version: 28
Download: download the raw HMM for this family

Species distribution

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

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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. 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 ACT domain has been found. There are 222 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 sequence.

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AlphaFold Structure Predictions

The list of proteins below match this family and have AlphaFold predicted structures. Click on the protein accession to view the predicted structure.

Protein Predicted structure External Information
A0A077ZDZ4 View 3D Structure Click here
A0A077ZHU6 View 3D Structure Click here
A0A077ZIM2 View 3D Structure Click here
A0A077ZNX0 View 3D Structure Click here
A0A096RY80 View 3D Structure Click here
A0A0D2DCM3 View 3D Structure Click here
A0A0D2ELY0 View 3D Structure Click here
A0A0D2FZX6 View 3D Structure Click here
A0A0H3GHZ9 View 3D Structure Click here
A0A0H3GNI7 View 3D Structure Click here
A0A0H3GQ40 View 3D Structure Click here
A0A0H3GUZ9 View 3D Structure Click here
A0A0N7KQ73 View 3D Structure Click here
A0A0P0W345 View 3D Structure Click here
A0A0P0WZL3 View 3D Structure Click here
A0A0P0X6M1 View 3D Structure Click here
A0A0P0Y131 View 3D Structure Click here
A0A0R0JM22 View 3D Structure Click here
A0A0R0KLJ8 View 3D Structure Click here
A0A0R0LK12 View 3D Structure Click here
A0A175W9U7 View 3D Structure Click here
A0A175WCH9 View 3D Structure Click here
A0A1C1CJ20 View 3D Structure Click here
A0A1C1D1R0 View 3D Structure Click here
A0A1D6ECE3 View 3D Structure Click here
A0A1D6F177 View 3D Structure Click here
A0A1D6GI89 View 3D Structure Click here
A0A1D6I1D8 View 3D Structure Click here
A0A1D6IA57 View 3D Structure Click here
A0A1D6JW11 View 3D Structure Click here
A0A1D6K5N4 View 3D Structure Click here
A0A1D6KK85 View 3D Structure Click here
A0A1D6KK86 View 3D Structure Click here
A0A1D6KNM8 View 3D Structure Click here
A0A1D6KWQ0 View 3D Structure Click here
A0A1D6L327 View 3D Structure Click here
A0A1D6LEL4 View 3D Structure Click here
A0A1D6LHN4 View 3D Structure Click here
A0A1D6MSC5 View 3D Structure Click here
A0A1D6PET7 View 3D Structure Click here