9D4T

Structure of HKU5-20s spike glycoprotein

Summary for 9D4T

• Entry DOI: 10.2210/pdb9d4t/pdb
• EMDB information: 46569
• Descriptor: Spike glycoprotein, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
• Functional Keywords: merbecovirus, hku5, hku5-20s, spike, viral protein
• Biological source: Pipistrellus bat coronavirus HKU5
• Total number of polymer chains: 3
• Total formula weight: 459344.92

Authors

Wu, Z.,Fan, C.,Bjorkman, P.J. (deposition date: 2024-08-12, release date: 2025-06-04, Last modification date: 2025-06-11)

Primary citation

Catanzaro, N.J.,Wu, Z.,Fan, C.,Jefferson, V.,Abdelgadir, A.,Schafer, A.,Yount, B.L.,Bjorkman, P.J.,Baric, R.,Letko, M.
ACE2 from Pipistrellus abramus bats is a receptor for HKU5 coronaviruses.
Nat Commun, 16:4932-4932, 2025

PubMed Abstract: The merbecovirus subgenus of coronaviruses includes Middle East Respiratory Syndrome Coronavirus (MERS-CoV), a zoonotic pathogen transmitted from dromedary camels to humans that causes severe respiratory disease. Viral discovery efforts uncover hundreds of merbecoviruses in different species across multiple continents, but few are studied under laboratory conditions, leaving basic questions regarding their human threat potential unresolved. Viral entry into host cells is a critical step for transmission between hosts. Here, we develop and apply a scalable approach to assesses novel merbecovirus cell entry across the entire merbecovirus subgenus. Merbecoviruses are sorted into clades based on the receptor-binding domain of the spike glycoprotein. Receptor tropism is clade-specific, with the clade including MERS-CoV using DPP4 and multiple clades using ACE2, including HKU5 bat coronaviruses. Mutational analysis identifies possible structural limitations to HKU5 adaptability and a cryo-EM structure of the HKU5-20s spike trimer reveals only 'down' RBDs.

PubMed: 40436893
DOI: 10.1038/s41467-025-60286-3

Experimental method

ELECTRON MICROSCOPY (2.8 Å)