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350  structures 5513  species 0  interactions 44729  sequences 72  architectures

Family: ACR_tran (PF00873)

Summary: AcrB/AcrD/AcrF family

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 "Acriflavine resistance protein family". More...

Acriflavine resistance protein family Edit Wikipedia article

ACR_tran
PDB 1oye EBI.jpg
structural basis of multiple binding capacity of the acrb multidrug efflux pump
Identifiers
SymbolACR_tran
PfamPF00873
Pfam clanCL0322
InterProIPR001036
SCOP21oy6 / SCOPe / SUPFAM
TCDB2.A.6
OPM superfamily16
OPM protein2gif

The Escherichia coli Acriflavine resistance (acrA and acrB genes) encode a multi-drug efflux system that is believed to protect the bacterium against hydrophobic inhibitors.[1] The E. coli AcrB protein is a transporter that is energized by proton-motive force and that shows the widest substrate specificity among all known multidrug pumps, ranging from most of the currently used antibiotics, disinfectants, dyes, and detergents to simple solvents.

The structure of ligand-free AcrB shows that it is a homotrimer of 110kDa per subunit. Each subunit contains 12 transmembrane helices and two large periplasmic domains (each exceeding 300 residues) between helices 1 and 2, and helices 7 and 8. X-ray analysis of the overexpressed AcrB protein demonstrated that the three periplasmic domains form, in the centre, a funnel-like structure and a connected narrow (or closed) pore. The pore is opened to the periplasm through three vestibules located at subunit interfaces. These vestibules were proposed to allow direct access of drugs from the periplasm as well as the outer leaflet of the cytoplasmic membrane. The three transmembrane domains of AcrB protomers form a large, 30A-wide central cavity that spans the cytoplasmic membrane and extends to the cytoplasm

X-ray crystallographic structures of the trimeric AcrB pump from E. coli with four structurally diverse ligands demonstrated that three molecules of ligand bind simultaneously to the extremely large central cavity of 5000 cubic angstroms, primarily by hydrophobic, aromatic stacking and van der Waals interactions. Each ligand uses a slightly different subset of AcrB residues for binding. The bound ligand molecules often interact with each other, stabilising the binding.

References

  1. ^ Ma D, Cook DN, Alberti M, Pon NG, Nikaido H, Hearst JE (1993). "Molecular cloning and characterization of acrA and acrE genes of Escherichia coli". J. Bacteriol. 175 (19): 6299–313. PMC 206727. PMID 8407802. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
This article incorporates text from the public domain Pfam and InterPro: IPR001036

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.

AcrB/AcrD/AcrF family Provide feedback

Members of this family are integral membrane proteins. Some are involved in drug resistance. AcrB cooperates with a membrane fusion protein, AcrA, and an outer membrane channel TolC. The structure shows the AcrB forms a homotrimer [1].

Literature references

  1. Murakami S, Nakashima R, Yamashita E, Yamaguchi A; , Nature 2002;419:587-593.: Crystal structure of bacterial multidrug efflux transporter AcrB. PUBMED:12374972 EPMC:12374972


Internal database links

External database links

This tab holds annotation information from the InterPro database.

InterPro entry IPR001036

The Escherichia coli acrA and acrB genes encode a multi-drug efflux system that is believed to protect the bacterium against hydrophobic inhibitors [ PUBMED:8407802 ]. The E. coli AcrB protein is a transporter that is energized by proton-motive force and that shows the widest substrate specificity among all known multidrug pumps, ranging from most of the currently used antibiotics, disinfectants, dyes, and detergents to simple solvents.

The structure of ligand-free AcrB shows that it is a homotrimer of 110kDa per subunit. Each subunit contains 12 transmembrane helices and two large periplasmic domains (each exceeding 300 residues) between helices 1 and 2, and helices 7 and 8. X-ray analysis of the overexpressed AcrB protein demonstrated that the three periplasmic domains form, in the centre, a funnel-like structure and a connected narrow (or closed) pore. The pore is opened to the periplasm through three vestibules located at subunit interfaces. These vestibules were proposed to allow direct access of drugs from the periplasm as well as the outer leaflet of the cytoplasmic membrane. The three transmembrane domains of AcrB protomers form a large, 30A-wide central cavity that spans the cytoplasmic membrane and extends to the cytoplasm

X-ray crystallographic structures of the trimeric AcrB pump from E. coli with four structurally diverse ligands demonstrated that three molecules of ligand bind simultaneously to the extremely large central cavity of 5000 cubic angstroms, primarily by hydrophobic, aromatic stacking and van der Waals interactions. Each ligand uses a slightly different subset of AcrB residues for binding. The bound ligand molecules often interact with each other, stabilising the binding.

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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Pfam Clan

This family is a member of clan RND_permease (CL0322), which has the following description:

Different members of the RND superfamily have been shown to transport hydrophobic drugs, fatty acids, bile salts, organic solvents, heavy metals, autoinducers and lipooligosaccharides in bacteria [1].

The clan contains the following 5 members:

ACR_tran MMPL Patched SecD_SecF Sterol-sensing

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...

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
(15)
Full
(44729)
Representative proteomes UniProt
(251052)
RP15
(5818)
RP35
(21023)
RP55
(46419)
RP75
(86253)
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HTML View             
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
(15)
Full
(44729)
Representative proteomes UniProt
(251052)
RP15
(5818)
RP35
(21023)
RP55
(46419)
RP75
(86253)
Alignment:
Format:
Order:
Sequence:
Gaps:
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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
(15)
Full
(44729)
Representative proteomes UniProt
(251052)
RP15
(5818)
RP35
(21023)
RP55
(46419)
RP75
(86253)
Raw Stockholm Download     Download   Download        
Gzipped 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: Pfam-B_578 (release 3.0)
Previous IDs: none
Type: Family
Sequence Ontology: SO:0100021
Author: Bateman A
Number in seed: 15
Number in full: 44729
Average length of the domain: 864.1 aa
Average identity of full alignment: 23 %
Average coverage of the sequence by the domain: 95.66 %

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 28.0 28.0
Trusted cut-off 28.0 28.0
Noise cut-off 27.9 27.9
Model length: 1021
Family (HMM) version: 22
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

Selections

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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 ACR_tran domain has been found. There are 350 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
A0A077ZGS5 View 3D Structure Click here
A0A0H3GNP4 View 3D Structure Click here
A0A0H3GPK5 View 3D Structure Click here
A0A0H3GQR4 View 3D Structure Click here
A0A0H3GR27 View 3D Structure Click here
A0A0H3GTZ3 View 3D Structure Click here
A0A0H3GU53 View 3D Structure Click here
A0A0H3GUM9 View 3D Structure Click here
A0A0H3GVW5 View 3D Structure Click here
A0A0H3GW07 View 3D Structure Click here
A0A0H3GYW5 View 3D Structure Click here
A6TBH4 View 3D Structure Click here
A6TBH5 View 3D Structure Click here
A8AEE5 View 3D Structure Click here
A8AEE6 View 3D Structure Click here
A9MKW9 View 3D Structure Click here
A9MKX0 View 3D Structure Click here
B2VFQ4 View 3D Structure Click here
B4EYA1 View 3D Structure Click here
C5BHN3 View 3D Structure Click here
D3V7P3 View 3D Structure Click here
D3V7P4 View 3D Structure Click here
G3XCW2 View 3D Structure Click here
O25328 View 3D Structure Click here
O25622 View 3D Structure Click here
O25887 View 3D Structure Click here
O31501 View 3D Structure Click here
P13511 View 3D Structure Click here
P24177 View 3D Structure Click here
P24181 View 3D Structure Click here
P25197 View 3D Structure Click here
P31224 View 3D Structure Click here
P37637 View 3D Structure Click here
P37972 View 3D Structure Click here
P38054 View 3D Structure Click here
P52002 View 3D Structure Click here
P76398 View 3D Structure Click here
P76399 View 3D Structure Click here
Q0P9L9 View 3D Structure Click here
Q0PBE4 View 3D Structure Click here