H. acinonychis diverged from H. pylori ~200,000 years ago via a host jump to large felines .
The atpB gene is highly conserved between H. acinonychis and H. pylori, with ~92% sequence identity .
Strain Sheeba retains functional atpB despite extensive gene fragmentation in other loci (e.g., vacA, cagPAI) .
No frameshifts or premature stop codons observed in atpB, unlike ~8% of other genes in H. acinonychis .
Subunit a partners with subunits b, b', and c to form the F0 proton channel .
Critical for maintaining proton motive force and ATP synthesis in acidic gastric environments .
Used to investigate ATP synthase inhibition as a potential therapeutic strategy .
Enables comparative studies of energy metabolism in Helicobacter species .
Serves as an antigen in ELISA for detecting H. acinonychis infections in captive felines .
Facilitates structural biology efforts to map bacterial ATP synthase mechanisms .
Function: A key component of the proton channel, directly involved in proton translocation across the membrane.
KEGG: hac:Hac_1196
STRING: 382638.Hac_1196