Summary: 4Fe-4S dicluster domain
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This is the Wikipedia entry entitled "Iron-sulfur protein". More...
Iron-sulfur protein Edit Wikipedia article
Iron-sulfur proteins are characterized by the presence of polymetallic systems containing sulfide ions, in which the iron ions have variable oxidation states. The simplest polymetallic system, [Fe2S2], is constituted by two iron ions bridged by two sulfide ions and coordinated by four cysteinyl ligands (in Fe2S2 ferredoxins) or by two cysteines and two histidines (in Rieske proteins). The oxidized proteins contain two Fe3+ ions, whereas the reduced proteins contain one Fe3+ and one Fe2+ ion.
Another common polymetallic system, [Fe4S4], consists of four iron ions and four sulfide ions placed at the vertices of a cubane-type structure, coordinated by four cysteinyl ligands. The [Fe4S4] electron-transfer proteins ([Fe4S4] ferredoxins) may be further subdivided into low-potential (bacterial-type) and high-potential (HiPIP) ferredoxins.
Low- and high-potential ferredoxins are related by the following redox scheme:
High-potential ferredoxins | ||||
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[Fe4S4]3+ |
<=> |
[Fe4S4]2+ |
<=> |
[Fe4S4]+ reduced |
Low-potential ferredoxins |
The formal oxidation numbers of the iron ions can be [2Fe3+, 2Fe2+] or [1Fe3+, 3Fe2+] in low-potential ferredoxins. The oxidation numbers of the iron ions in high-potential ferredoxins can be [3Fe3+, 1Fe2+] or [2Fe3+, 2Fe2+].
There also are proteins containing an [Fe3S4] centre, in which one iron is missing from the [Fe4S4] core. Three sulfide ions bridge two iron ions each, while the fourth sulfide bridges three iron ions. Their formal oxidation states may vary from [Fe3S4]+ (all-Fe3+ form) to [Fe3S4]2- (all-Fe2+ form). In a number of iron-sulfur proteins, the [Fe4S4] cluster can be reversibly converted by oxidation and loss of one iron ion to a [Fe3S4] cluster. E.g., the inactive form of aconitase possesses an [Fe3S4] and is activated by addition of Fe2+ and reductant.
More complex polymetallic systems are found in nitrogenase and hydrogenase.
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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.
4Fe-4S dicluster domain Provide feedback
This family includes proteins containing domains which bind to iron-sulfur clusters. Members include bacterial ferredoxins, various dehydrogenases, and various reductases. The structure of the domain is an alpha-antiparallel beta sandwich.
Internal database links
SCOOP: | DUF362 Fer4 Fer4_11 Fer4_12 Fer4_16 Fer4_17 Fer4_2 Fer4_21 Fer4_22 Fer4_4 Fer4_6 Fer4_7 Fer4_8 Fer4_9 Radical_SAM |
Similarity to PfamA using HHSearch: | Fer4 Fer4 Fer4_2 Fer4_3 Fer4_6 Fer4_7 Fer4_7 Fer4_8 Fer4_8 Fer4_9 Fer4_9 Fer4_10 Fer4_10 Fer4_16 Fer4_16 Fer4_17 Fer4_17 Fer4_21 Fer4_21 |
This tab holds annotation information from the InterPro database.
InterPro entry IPR017896
Ferredoxins are a group of iron-sulphur proteins which mediate electron transfer in a wide variety of metabolic reactions. Ferredoxins can be divided into several subgroups depending upon the physiological nature of the iron-sulphur cluster(s). One of these subgroups are the 4Fe-4S ferredoxins, which are found in bacteria and which are thus often referred as 'bacterial-type' ferredoxins. The structure of these proteins [ PUBMED:3129571 ] consists of the duplication of a domain of twenty six amino acid residues; each of these domains contains four cysteine residues that bind to a 4Fe-4S centre.
Several structures of the 4Fe-4S ferredoxin domain have been determined [ PUBMED:7966291 ]. The clusters consist of two interleaved 4Fe- and 4S-tetrahedra forming a cubane-like structure, in such a way that the four iron occupy the eight corners of a distorted cube. Each 4Fe-4S is attached to the polypeptide chain by four covalent Fe-S bonds involving cysteine residues.
A number of proteins have been found [ PUBMED:2185975 ] that include one or more 4Fe-4S binding domains similar to those of bacterial-type ferredoxins.
The pattern of cysteine residues in the iron-sulphur region is sufficient to detect this class of 4Fe-4S binding proteins. This entry represents the whole domain.
Note:In some bacterial ferredoxins, one of the two duplicated domains has lost one or more of the four conserved cysteines. The consequence of such variations is that these domains have either lost their iron-sulphur binding property or bind to a 3Fe-3S centre instead of a 4Fe-4S centre.
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 4Fe-4S (CL0344), which has the following description:
Superfamily includes proteins containing domains which bind to iron-sulfur clusters. Members include bacterial ferredoxins, various dehydrogenases and various reductases. The structure of the domain is an alpha-antiparallel beta sandwich.
The clan contains the following 29 members:
ETF_QO Fer4 Fer4_10 Fer4_11 Fer4_12 Fer4_13 Fer4_14 Fer4_15 Fer4_16 Fer4_17 Fer4_18 Fer4_19 Fer4_2 Fer4_20 Fer4_21 Fer4_22 Fer4_23 Fer4_24 Fer4_3 Fer4_4 Fer4_5 Fer4_6 Fer4_7 Fer4_8 Fer4_9 FeS Molybdop_Fe4S4 Nitr_red_alph_N RLIAlignments
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 (11) |
Full (3263) |
Representative proteomes | UniProt (16197) |
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RP15 (378) |
RP35 (1459) |
RP55 (3360) |
RP75 (6152) |
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Jalview | |||||||
HTML | |||||||
PP/heatmap | 1 |
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
available,
not generated,
— not available.
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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 (11) |
Full (3263) |
Representative proteomes | UniProt (16197) |
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RP15 (378) |
RP35 (1459) |
RP55 (3360) |
RP75 (6152) |
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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: | Jackhmmer:Q5FDF3 |
Previous IDs: | none |
Type: | Domain |
Sequence Ontology: | SO:0000417 |
Author: |
Coggill P |
Number in seed: | 11 |
Number in full: | 3263 |
Average length of the domain: | 101.7 aa |
Average identity of full alignment: | 53 % |
Average coverage of the sequence by the domain: | 22.72 % |
HMM information
HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 61295632 -E 1000 --cpu 4 HMM pfamseq
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Model details: |
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Model length: | 114 | ||||||||||||
Family (HMM) version: | 9 | ||||||||||||
Download: | download the raw HMM for this family |
Species distribution
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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 |
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O26038 | View 3D Structure | Click here |
P18396 | View 3D Structure | Click here |
P54932 | View 3D Structure | Click here |
Q01854 | View 3D Structure | Click here |
Q0PBE1 | View 3D Structure | Click here |
Q5F7Y5 | View 3D Structure | Click here |
Q9HWQ0 | View 3D Structure | Click here |
Q9I3G6 | View 3D Structure | Click here |