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7R6P

Solution structure of peptide toxin MIITX2-Mg1a from the venom of the Australian giant red bull ant Myrmecia gulosa

Summary for 7R6P
Entry DOI10.2210/pdb7r6p/pdb
NMR InformationBMRB: 30928
DescriptorU-myrmeciitoxin(02)-Mg1a (1 entity in total)
Functional Keywordsmolecular mimicry, chemical mimicry, epidermal growth factor receptor, hormone, convergent evolution, venom toxin, toxin
Biological sourceMyrmecia gulosa (Red bulldog ant)
Total number of polymer chains1
Total formula weight5861.39
Authors
Chin, Y.K.,Eagle, D.,Bankala, K.,Robinson, S.D. (deposition date: 2021-06-23, release date: 2022-02-09, Last modification date: 2024-10-23)
Primary citationEagles, D.A.,Saez, N.J.,Krishnarjuna, B.,Bradford, J.J.,Chin, Y.K.,Starobova, H.,Mueller, A.,Reichelt, M.E.,Undheim, E.A.B.,Norton, R.S.,Thomas, W.G.,Vetter, I.,King, G.F.,Robinson, S.D.
A peptide toxin in ant venom mimics vertebrate EGF-like hormones to cause long-lasting hypersensitivity in mammals.
Proc.Natl.Acad.Sci.USA, 119:-, 2022
Cited by
PubMed Abstract: Venoms are excellent model systems for studying evolutionary processes associated with predator-prey interactions. Here, we present the discovery of a peptide toxin, MIITX-Mg1a, which is a major component of the venom of the Australian giant red bull ant and has evolved to mimic, both structurally and functionally, vertebrate epidermal growth factor (EGF) peptide hormones. We show that Mg1a is a potent agonist of the mammalian EGF receptor ErbB1, and that intraplantar injection in mice causes long-lasting hypersensitivity of the injected paw. These data reveal a previously undescribed venom mode of action, highlight a role for ErbB receptors in mammalian pain signaling, and provide an example of molecular mimicry driven by defensive selection pressure.
PubMed: 35131940
DOI: 10.1073/pnas.2112630119
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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