9ZFU image
Deposition Date 2025-12-02
Release Date 2026-10-14
Last Version Date 2026-10-14
Entry Detail
PDB ID:
9ZFU
Keywords:
Title:
F1 ATPase from Acanthamoeba castellanii
Biological Source:
Source Organism(s):
Method Details:
Experimental Method:
Resolution:
3.77 Å
Aggregation State:
PARTICLE
Reconstruction Method:
SINGLE PARTICLE
Macromolecular Entities
Polymer Type:polypeptide(L)
Molecule:ATP synthase gamma subunit, m
Chain IDs:A
Chain Length:326
Number of Molecules:1
Biological Source:Acanthamoeba castellanii
Polymer Type:polypeptide(L)
Molecule:ATP synthase inhibitory facto
Chain IDs:H (auth: B)
Chain Length:137
Number of Molecules:1
Biological Source:Acanthamoeba castellanii
Polymer Type:polypeptide(L)
Molecule:ATP synthase subunit alpha, m
Gene (Uniprot):ATP1
Chain IDs:B (auth: R), C (auth: S), D (auth: T)
Chain Length:522
Number of Molecules:3
Biological Source:Acanthamoeba castellanii
Polymer Type:polypeptide(L)
Molecule:ATP synthase subunit beta
Gene (Uniprot):ACA1_367940
Chain IDs:E (auth: U), F (auth: V), G (auth: W)
Chain Length:687
Number of Molecules:3
Biological Source:Acanthamoeba castellanii
Primary Citation
Acanthamoeba ATP synthase structure reveals the TCA cycle is tethered to OXPHOS.
Cell 189 6307 6324.e7 (2026)
PMID: 42822427 DOI: 10.1016/j.cell.2026.08.057

Abstact

Oxidative phosphorylation (OXPHOS) is a key metabolic process that couples redox energy to ATP production. While some core OXPHOS complex subunits are found across all domains of life, many have diverged or expanded across evolution-as seen in the protozoan pathogen Acanthamoeba castellanii. By integrating cryo-electron microscopy of unenriched mitochondrial lysate with mass spectrometry proteomics, we resolved the structures of endogenous mitochondrial ATP synthase (complex V), Hsp60, and respiratory complex III from Acanthamoeba. We capture Acanthamoeba ATP synthase in an IF1-inhibited state and reveal how Acanthamoeba-specific subunits and extensions stabilize the molecular machine, which includes a beta subunit extension that interfaces with the peripheral stalk. Additionally, we characterize an active malate dehydrogenase (MDH) dimer structurally integrated within the ATP synthase peripheral stalk, thus revealing a direct protein tether between OXPHOS and the tricarboxylic acid cycle. Together, these findings provide structural insight into lineage-specific adaptations in Acanthamoeba that may tune protozoan metabolism.

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Primary Citation of related structures
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