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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | ADP-bound structure of PmtCD in peptidisc | |||||||||
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Keywords | ABC transporter / MEMBRANE PROTEIN | |||||||||
| Function / homology | Function and homology informationABC-type transporter activity / ATP hydrolysis activity / ATP binding / plasma membrane Similarity search - Function | |||||||||
| Biological species | ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 4.2 Å | |||||||||
Authors | Worrall LJ / Li FKK / Hu J / Lazarski AC / Strynadka NCJ | |||||||||
| Funding support | Canada, 1 items
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Citation | Journal: Commun Biol / Year: 2025Title: Cryo-EM analysis of the Staphylococcus aureus phenol-soluble modulin exporter PmtCD apo form in detergent micelles, nanodiscs and peptidiscs. Authors: Jinhong Hu / Aleksander C Lazarski / Franco K K Li / Liam J Worrall / Dylan J Burgin / Natalie Zeytuni / Seth W Dickey / Michael Otto / Natalie C J Strynadka / ![]() Abstract: Staphylococci secrete amphipathic peptides known as phenol soluble modulins (PSMs) that play a variety of pathogenic roles including host cell membrane destruction, biofilm development, and the ...Staphylococci secrete amphipathic peptides known as phenol soluble modulins (PSMs) that play a variety of pathogenic roles including host cell membrane destruction, biofilm development, and the triggering of inflammatory responses. PSM export is facilitated by the essential ATP-binding cassette (ABC) transporter PmtCD, which also provides producer immunity toward the membrane-damaging PSMs. Here, we report cryo-EM structures of PmtCD in a nucleotide-free state using different membrane mimetics - detergent, nanodisc and peptidisc - all featuring the transmembrane domains in an open state with a remarkably expansive intervening lumen. The consistently sized lumen suggests the possibility for two α-helical amphipathic PSMs to pack and passage within. A continuous hydrophobic surface with no apparent single high affinity site is in keeping with the ability of PmtCD to export a variety of hydrophobic PSM peptide substrates. The ATP driven collapse of the PmtD lumen is consistent with the lateral access and extrusion mechanisms of related ABC transporters that translocate membrane embedded substrates. Along with a new ADP product complex and prior ATPγS-bound form, these structures provide insights into the export of PSMs and a foundation for design of trojan horse antimicrobials that target MRSA strains from within by blocking membranolytic PSM export. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_72173.map.gz | 2 MB | EMDB map data format | |
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| Header (meta data) | emd-72173-v30.xml emd-72173.xml | 18.1 KB 18.1 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_72173_fsc.xml | 6.1 KB | Display | FSC data file |
| Images | emd_72173.png | 90.2 KB | ||
| Filedesc metadata | emd-72173.cif.gz | 6.1 KB | ||
| Others | emd_72173_half_map_1.map.gz emd_72173_half_map_2.map.gz | 14.3 MB 14.3 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-72173 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-72173 | HTTPS FTP |
-Validation report
| Summary document | emd_72173_validation.pdf.gz | 689.6 KB | Display | EMDB validaton report |
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| Full document | emd_72173_full_validation.pdf.gz | 689.2 KB | Display | |
| Data in XML | emd_72173_validation.xml.gz | 11.6 KB | Display | |
| Data in CIF | emd_72173_validation.cif.gz | 16.2 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-72173 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-72173 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9q2rMC ![]() 9q1yC ![]() 9q2nC ![]() 9q2qC C: citing same article ( M: atomic model generated by this map |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_72173.map.gz / Format: CCP4 / Size: 18.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.35 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #1
| File | emd_72173_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #2
| File | emd_72173_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Hetero tetrameric complex of PmtC (2) and PmtD (2)
| Entire | Name: Hetero tetrameric complex of PmtC (2) and PmtD (2) |
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| Components |
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-Supramolecule #1: Hetero tetrameric complex of PmtC (2) and PmtD (2)
| Supramolecule | Name: Hetero tetrameric complex of PmtC (2) and PmtD (2) / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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| Source (natural) | Organism: ![]() |
-Macromolecule #1: Phenol-soluble modulin export ABC transporter permease subunit PmtD
| Macromolecule | Name: Phenol-soluble modulin export ABC transporter permease subunit PmtD type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 28.631359 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: VPRGSHRILN LVKYDLYSIF KSPLTYLAIL VVSSLIATQS ILMANSMDNP KHIIVYGSVF AAAKWLLLII GLMFVVKTIT RDFSQGTIQ LYMSKVKTRV GYIISKTISI ILISILFALI HYVILIVVQA SSNGKNLAFS KYVDNLWFFL IFLLFFGLFL F LITLASQK ...String: VPRGSHRILN LVKYDLYSIF KSPLTYLAIL VVSSLIATQS ILMANSMDNP KHIIVYGSVF AAAKWLLLII GLMFVVKTIT RDFSQGTIQ LYMSKVKTRV GYIISKTISI ILISILFALI HYVILIVVQA SSNGKNLAFS KYVDNLWFFL IFLLFFGLFL F LITLASQK TAMIFSLGVF LVLIVPFIKP FITFIPRYGE KVLDAFDYIP FAYLTDKMIS SNFDFSNWQW VISLGSIVIF FI LNILYVA KKDI UniProtKB: Phenol-soluble modulin export ABC transporter permease subunit PmtD |
-Macromolecule #2: ABC transporter ATP-binding protein
| Macromolecule | Name: ABC transporter ATP-binding protein / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 33.001098 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MKLEHITKKY GSNVVLNDID FDFGDSRIVG LIGKNGVGKT TVMKVMNGNI IKFDGKVDID NADNIGFLIE HPKLYDNKSG LYNLKLFAQ VLGKGFDKAY TDKIIDAFGM RPYIKKKVKK YSMGMKQKLA IAVSLMNKPK FLILDEPTNG MDPDGSIDVL T TIKSLVNE ...String: MKLEHITKKY GSNVVLNDID FDFGDSRIVG LIGKNGVGKT TVMKVMNGNI IKFDGKVDID NADNIGFLIE HPKLYDNKSG LYNLKLFAQ VLGKGFDKAY TDKIIDAFGM RPYIKKKVKK YSMGMKQKLA IAVSLMNKPK FLILDEPTNG MDPDGSIDVL T TIKSLVNE LDMRILISSH KLEDIELICD RAVFLRDGHF VQDVNMEEGV ASDTTIVTVD HKDFDRTEKY LAEHFQLQNV DK ADGHLMI NAQKNYQVIL KALSELDIYP KYIETRKSSL RDTYFNINQR GDK UniProtKB: ABC transporter ATP-binding protein |
-Macromolecule #3: ADENOSINE-5'-DIPHOSPHATE
| Macromolecule | Name: ADENOSINE-5'-DIPHOSPHATE / type: ligand / ID: 3 / Number of copies: 2 / Formula: ADP |
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| Molecular weight | Theoretical: 427.201 Da |
| Chemical component information | ![]() ChemComp-ADP: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 8.8 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.5 µm / Nominal defocus min: 1.5 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi




Keywords
Authors
Canada, 1 items
Citation









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Processing
FIELD EMISSION GUN


