6N2D image
Deposition Date 2018-11-12
Release Date 2019-02-20
Last Version Date 2024-03-20
Entry Detail
PDB ID:
6N2D
Keywords:
Title:
Bacillus PS3 ATP synthase membrane region
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
3.30 Å
Aggregation State:
PARTICLE
Reconstruction Method:
SINGLE PARTICLE
Macromolecular Entities
Polymer Type:polypeptide(L)
Molecule:ATP synthase subunit a
Chain IDs:C (auth: a)
Chain Length:237
Number of Molecules:1
Biological Source:Bacillus sp. PS3
Polymer Type:polypeptide(L)
Molecule:ATP synthase subunit b
Chain IDs:A (auth: b2), B (auth: b1)
Chain Length:167
Number of Molecules:2
Biological Source:Bacillus sp. PS3
Polymer Type:polypeptide(L)
Molecule:ATP synthase subunit c
Gene (Uniprot):atpE
Chain IDs:D (auth: c0), E (auth: c1), F (auth: c2), G (auth: c3), H (auth: c4), I (auth: c5), J (auth: c6), K (auth: c7), L (auth: c8), M (auth: c9)
Chain Length:72
Number of Molecules:10
Biological Source:Bacillus sp. PS3
Ligand Molecules
Primary Citation
Structure of a bacterial ATP synthase.
Elife 8 ? ? (2019)
PMID: 30724163 DOI: 10.7554/eLife.43128

Abstact

ATP synthases produce ATP from ADP and inorganic phosphate with energy from a transmembrane proton motive force. Bacterial ATP synthases have been studied extensively because they are the simplest form of the enzyme and because of the relative ease of genetic manipulation of these complexes. We expressed the Bacillus PS3 ATP synthase in Eschericia coli, purified it, and imaged it by cryo-EM, allowing us to build atomic models of the complex in three rotational states. The position of subunit ε shows how it is able to inhibit ATP hydrolysis while allowing ATP synthesis. The architecture of the membrane region shows how the simple bacterial ATP synthase is able to perform the same core functions as the equivalent, but more complicated, mitochondrial complex. The structures reveal the path of transmembrane proton translocation and provide a model for understanding decades of biochemical analysis interrogating the roles of specific residues in the enzyme.

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Primary Citation of related structures
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