8YHO
Cryo-EM structure of the trimeric HerA
Summary for 8YHO
| Entry DOI | 10.2210/pdb8yho/pdb |
| EMDB information | 39290 |
| Descriptor | DUF87 domain-containing protein (1 entity in total) |
| Functional Keywords | antiphage system, immune system |
| Biological source | Staphylococcus aureus |
| Total number of polymer chains | 3 |
| Total formula weight | 195765.50 |
| Authors | |
| Primary citation | Zhen, X.,Zhou, B.,Liu, Z.,Wang, X.,Zhao, H.,Wu, S.,Li, Z.,Liang, J.,Zhang, W.,Zhu, Q.,He, J.,Xiong, X.,Ouyang, S. Mechanistic basis for the allosteric activation of NADase activity in the Sir2-HerA antiphage defense system. Nat Commun, 15:9269-9269, 2024 Cited by PubMed Abstract: Sir2-HerA is a widely distributed antiphage system composed of a RecA-like ATPase (HerA) and an effector with potential NADase activity (Sir2). Sir2-HerA is believed to provide defense against phage infection in Sir2-dependent NAD depletion to arrest the growth of infected cells. However, the detailed mechanism underlying its antiphage activity remains largely unknown. Here, we report functional investigations of Sir2-HerA from Staphylococcus aureus (SaSir2-HerA), unveiling that the NADase function of SaSir2 can be allosterically activated by the binding of SaHerA, which then assembles into a supramolecular complex with NADase activity. By combining the cryo-EM structure of SaSir2-HerA in complex with the NAD cleavage product, it is surprisingly observed that Sir2 protomers that interact with HerA are in the activated state, which is due to the opening of the α15-helix covering the active site, allowing NAD to access the catalytic pocket for hydrolysis. In brief, our study provides a comprehensive view of an allosteric activation mechanism for Sir2 NADase activity in the Sir2-HerA immune system. PubMed: 39465277DOI: 10.1038/s41467-024-53614-6 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (2.8 Å) |
Structure validation
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