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 | |||||||||
---|---|---|---|---|---|---|---|---|---|
![]() crystal structure of e. coli aspartokinase iii in complex with aspartate and adp (r-state) | |||||||||
Identifiers | |||||||||
Symbol | ACT | ||||||||
Pfam | PF01842 | ||||||||
Pfam clan | CL0070 | ||||||||
InterPro | IPR002912 | ||||||||
SCOP2 | 1psd / 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
- ^ 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 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
-
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
-
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
SCOOP: | ACT_4 ACT_5 ACT_6 ACT_7 ACT_8 Pkinase_fungal Saccharop_dh_N |
Similarity to PfamA using HHSearch: | ACT_4 ACT_5 ACT_6 ACT_7 |
External database links
HOMSTRAD: | ACT |
SCOP: | 1psd |
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...
Loading domain graphics...
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_CAlignments
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...
View options
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) |
||||
Jalview | |||||||
HTML | |||||||
PP/heatmap | 1 |
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
available,
not generated,
— not available.
Format an alignment
Download options
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 | |||||||
Gzipped |
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
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
HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 61295632 -E 1000 --cpu 4 HMM pfamseq
|
||||||||||||
Model details: |
|
||||||||||||
Model length: | 66 | ||||||||||||
Family (HMM) version: | 28 | ||||||||||||
Download: | download the raw HMM for this family |
Species distribution
Sunburst controls
HideWeight segments by...
Change the size of the sunburst
Colour assignments
![]() |
![]() |
![]() |
![]() |
![]() |
![]() |
![]() |
![]() |
Selections
Generate a FASTA-format file
Clear selection
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...
Tree controls
HideThe tree shows the occurrence of this domain across different species. More...
Loading...
Please note: for large trees this can take some time. While the tree is loading, you can safely switch away from this tab but if you browse away from the family page entirely, the tree will not be loaded.
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.
Loading structure mapping...
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.