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7RUG

Human SERINC3-DeltaICL4

Summary for 7RUG
Entry DOI10.2210/pdb7rug/pdb
EMDB information24698 24705
DescriptorSerine incorporator 3, SiA (2 entities in total)
Functional Keywordsflippase, viral restriction, hiv-1, unknown function
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight78101.55
Authors
Purdy, M.D.,Leonhardt, S.A.,Yeager, M. (deposition date: 2021-08-17, release date: 2022-08-24, Last modification date: 2023-09-06)
Primary citationLeonhardt, S.A.,Purdy, M.D.,Grover, J.R.,Yang, Z.,Poulos, S.,McIntire, W.E.,Tatham, E.A.,Erramilli, S.K.,Nosol, K.,Lai, K.K.,Ding, S.,Lu, M.,Uchil, P.D.,Finzi, A.,Rein, A.,Kossiakoff, A.A.,Mothes, W.,Yeager, M.
Antiviral HIV-1 SERINC restriction factors disrupt virus membrane asymmetry.
Nat Commun, 14:4368-4368, 2023
Cited by
PubMed Abstract: The host proteins SERINC3 and SERINC5 are HIV-1 restriction factors that reduce infectivity when incorporated into the viral envelope. The HIV-1 accessory protein Nef abrogates incorporation of SERINCs via binding to intracellular loop 4 (ICL4). Here, we determine cryoEM maps of full-length human SERINC3 and an ICL4 deletion construct, which reveal that hSERINC3 is comprised of two α-helical bundles connected by a ~ 40-residue, highly tilted, "crossmember" helix. The design resembles non-ATP-dependent lipid transporters. Consistently, purified hSERINCs reconstituted into proteoliposomes induce flipping of phosphatidylserine (PS), phosphatidylethanolamine and phosphatidylcholine. Furthermore, SERINC3, SERINC5 and the scramblase TMEM16F expose PS on the surface of HIV-1 and reduce infectivity, with similar results in MLV. SERINC effects in HIV-1 and MLV are counteracted by Nef and GlycoGag, respectively. Our results demonstrate that SERINCs are membrane transporters that flip lipids, resulting in a loss of membrane asymmetry that is strongly correlated with changes in Env conformation and loss of infectivity.
PubMed: 37474505
DOI: 10.1038/s41467-023-39262-2
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.7 Å)
Structure validation

227111

數據於2024-11-06公開中

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