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7ET3

C5 portal vertex in the enveloped virion capsid

Summary for 7ET3
Entry DOI10.2210/pdb7et3/pdb
EMDB information31297
DescriptorTriplex capsid protein 2, Large tegument protein deneddylase, Triplex capsid protein 1, ... (8 entities in total)
Functional Keywordsc5 portal vertex, enveloped capsid, viral protein
Biological sourceHuman cytomegalovirus (HHV-5, Human herpesvirus 5)
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Total number of polymer chains23
Total formula weight2002476.33
Authors
Li, Z.,Yu, X. (deposition date: 2021-05-12, release date: 2021-07-14, Last modification date: 2025-07-02)
Primary citationLi, Z.,Pang, J.,Dong, L.,Yu, X.
Structural basis for genome packaging, retention, and ejection in human cytomegalovirus.
Nat Commun, 12:4538-4538, 2021
Cited by
PubMed Abstract: How the human cytomegalovirus (HCMV) genome-the largest among human herpesviruses-is packaged, retained, and ejected remains unclear. We present the in situ structures of the symmetry-mismatched portal and the capsid vertex-specific components (CVSCs) of HCMV. The 5-fold symmetric 10-helix anchor-uncommon among known portals-contacts the portal-encircling DNA, which is presumed to squeeze the portal as the genome packaging proceeds. We surmise that the 10-helix anchor dampens this action to delay the portal reaching a "head-full" packaging state, thus facilitating the large genome to be packaged. The 6-fold symmetric turret, latched via a coiled coil to a helix from a major capsid protein, supports the portal to retain the packaged genome. CVSCs at the penton vertices-presumed to increase inner capsid pressure-display a low stoichiometry, which would aid genome retention. We also demonstrate that the portal and capsid undergo conformational changes to facilitate genome ejection after viral cell entry.
PubMed: 34315863
DOI: 10.1038/s41467-021-24820-3
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.2 Å)
Structure validation

238895

数据于2025-07-16公开中

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