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7QTX

Kaposi sarcoma associated herpes virus (KSHV) encoded apoptosis inhibitor, KsBcl-2 in complex with Puma BH3

Summary for 7QTX
Entry DOI10.2210/pdb7qtx/pdb
DescriptorBcl-2, Bcl-2-binding component 3, isoforms 1/2, BROMIDE ION, ... (5 entities in total)
Functional Keywordsapoptosis, viral bcl-2 protein, gamma herpes virus, kaposi sarcoma virus
Biological sourceHuman gammaherpesvirus 8
More
Total number of polymer chains2
Total formula weight20273.62
Authors
Suraweera, C.D.,Hinds, M.G.,Kvansakul, M. (deposition date: 2022-01-17, release date: 2022-11-23, Last modification date: 2024-05-01)
Primary citationSuraweera, C.D.,Hinds, M.G.,Kvansakul, M.
Structural Insight into KsBcl-2 Mediated Apoptosis Inhibition by Kaposi Sarcoma Associated Herpes Virus.
Viruses, 14:-, 2022
Cited by
PubMed Abstract: Numerous large DNA viruses have evolved sophisticated countermeasures to hijack the premature programmed cell death of host cells post-infection, including the expression of proteins homologous in sequence, structure, or function to cellular Bcl-2 proteins. Kaposi sarcoma herpes virus (KSHV), a member of the , has been shown to encode for KsBcl-2, a potent inhibitor of Bcl-2 mediated apoptosis. KsBcl-2 acts by directly engaging host pro-apoptotic Bcl-2 proteins including Bak, Bax and Bok, the BH3-only proteins; Bim, Bid, Bik, Hrk, Noxa and Puma. Here we determined the crystal structures of KsBcl-2 bound to the BH3 motif of pro-apoptotic proteins Bid and Puma. The structures reveal that KsBcl-2 engages pro-apoptotic BH3 motif peptides using the canonical ligand binding groove. Thus, the presence of the readily identifiable conserved BH1 motif sequence "NWGR" of KsBcl-2, as well as highly conserved Arg residue (R86) forms an ionic interaction with the conserved Asp in the BH3 motif in a manner that mimics the canonical ionic interaction seen in host Bcl-2:BH3 motif complexes. These findings provide a structural basis for KSHV mediated inhibition of host cell apoptosis and reveal the flexibility of virus encoded Bcl-2 proteins to mimic key interactions from endogenous host signalling pathways.
PubMed: 35458468
DOI: 10.3390/v14040738
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.11598861103 Å)
Structure validation

227344

數據於2024-11-13公開中

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