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8BF5

Early transcription elongation state of influenza A/H7N9 polymerase stalled with incoming GTP analogue

Summary for 8BF5
Entry DOI10.2210/pdb8bf5/pdb
Related7QTL
EMDB information16013
DescriptorPolymerase acidic protein, RNA-directed RNA polymerase catalytic subunit, Polymerase basic protein 2, ... (9 entities in total)
Functional Keywordsinfluenza, viral rna-dependent rna polymerase; cap-dependent transcription, nucleoside analogue, viral protein
Biological sourceInfluenza B virus (B/Memphis/13/2003)
More
Total number of polymer chains6
Total formula weight281402.80
Authors
Cusack, S.,Kouba, T. (deposition date: 2022-10-24, release date: 2022-12-28, Last modification date: 2024-07-24)
Primary citationKouba, T.,Dubankova, A.,Drncova, P.,Donati, E.,Vidossich, P.,Speranzini, V.,Pflug, A.,Huchting, J.,Meier, C.,De Vivo, M.,Cusack, S.
Direct observation of backtracking by influenza A and B polymerases upon consecutive incorporation of the nucleoside analog T1106.
Cell Rep, 42:111901-111901, 2023
Cited by
PubMed Abstract: The antiviral pseudo-base T705 and its de-fluoro analog T1106 mimic adenine or guanine and can be competitively incorporated into nascent RNA by viral RNA-dependent RNA polymerases. Although dispersed, single pseudo-base incorporation is mutagenic, consecutive incorporation causes polymerase stalling and chain termination. Using a template encoding single and then consecutive T1106 incorporation four nucleotides later, we obtained a cryogenic electron microscopy structure of stalled influenza A/H7N9 polymerase. This shows that the entire product-template duplex backtracks by 5 nt, bringing the singly incorporated T1106 to the +1 position, where it forms an unexpected T1106:U wobble base pair. Similar structures show that influenza B polymerase also backtracks after consecutive T1106 incorporation, regardless of whether prior single incorporation has occurred. These results give insight into the unusual mechanism of chain termination by pyrazinecarboxamide base analogs. Consecutive incorporation destabilizes the proximal end of the product-template duplex, promoting irreversible backtracking to a more energetically favorable overall configuration.
PubMed: 36596301
DOI: 10.1016/j.celrep.2022.111901
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.96 Å)
Structure validation

227111

数据于2024-11-06公开中

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