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8ERF

HTLV-1 capsid protein N-terminal domain orthorhombic crystal form

Summary for 8ERF
Entry DOI10.2210/pdb8erf/pdb
Related8ERE
Descriptorcapsid protein p24, SULFATE ION (3 entities in total)
Functional Keywordscapsid, viral protein
Biological sourceHTLV-1 subtype C
Total number of polymer chains2
Total formula weight28386.05
Authors
Yu, R.J.,Li, N.,Jacques, D.A. (deposition date: 2022-10-11, release date: 2023-10-18, Last modification date: 2025-12-17)
Primary citationYu, R.,Phalora, P.,Li, N.,Bocking, T.,Jacques, D.A.
The Human T-cell Leukemia Virus capsid protein is a potential drug target.
Nat Commun, 16:10892-10892, 2025
Cited by
PubMed Abstract: Human T-cell Leukaemia Virus type 1 (HTLV-1) is an untreatable retrovirus that causes lethal malignancies and degenerative inflammatory conditions. Effective treatments have been delayed by substantial gaps in our knowledge of the fundamental virology, especially when compared to the closely related virus, HIV. A recently developed and highly effective anti-HIV strategy is to target the virus with drugs that interfere with capsid integrity and interactions with the host. Importantly, the first in-class anti-capsid drug approved, lenacapavir, can provide long-acting pre-exposure prophylaxis. Such a property would provide a means to prevent the transmission of HTLV-1, but its capsid has not previously been considered as a drug target. Here we describe high-resolution crystal structures of the HTLV-1 capsid protein, define essential lattice interfaces, and identify a distinct ligand-binding pocket. We show that this pocket is essential for virus infectivity, providing a potential target for future anti-capsid drug development.
PubMed: 41345105
DOI: 10.1038/s41467-025-65899-2
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.47 Å)
Structure validation

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PDB entries from 2025-12-31

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