[English] 日本語
Yorodumi Papers
- Database of articles cited by EMDB/PDB/SASBDB data -

+
Search query

Keywords
Structure methods
Author
Journal
IF

-
Structure paper

TitleMapping inhibitory sites on the RNA polymerase of the 1918 pandemic influenza virus using nanobodies.
Journal, issue, pagesNat Commun, Vol. 13, Issue 1, Page 251, Year 2022
Publish dateJan 11, 2022
AuthorsJeremy R Keown / Zihan Zhu / Loïc Carrique / Haitian Fan / Alexander P Walker / Itziar Serna Martin / Els Pardon / Jan Steyaert / Ervin Fodor / Jonathan M Grimes /
PubMed AbstractInfluenza A viruses cause seasonal epidemics and global pandemics, representing a considerable burden to healthcare systems. Central to the replication cycle of influenza viruses is the viral RNA- ...Influenza A viruses cause seasonal epidemics and global pandemics, representing a considerable burden to healthcare systems. Central to the replication cycle of influenza viruses is the viral RNA-dependent RNA polymerase which transcribes and replicates the viral RNA genome. The polymerase undergoes conformational rearrangements and interacts with viral and host proteins to perform these functions. Here we determine the structure of the 1918 influenza virus polymerase in transcriptase and replicase conformations using cryo-electron microscopy (cryo-EM). We then structurally and functionally characterise the binding of single-domain nanobodies to the polymerase of the 1918 pandemic influenza virus. Combining these functional and structural data we identify five sites on the polymerase which are sensitive to inhibition by nanobodies. We propose that the binding of nanobodies at these sites either prevents the polymerase from assuming particular functional conformations or interactions with viral or host factors. The polymerase is highly conserved across the influenza A subtypes, suggesting these sites as effective targets for potential influenza antiviral development.
External linksNat Commun / PubMed:35017564 / PubMed Central
MethodsEM (single particle) / X-ray diffraction
Resolution1.68 - 6.72 Å
Structure data

EMDB-12322, PDB-7nha:
1918 H1N1 Viral influenza polymerase heterotrimer - Endonuclease and priming loop ordered (Class2a)
Method: EM (single particle) / Resolution: 2.91 Å

EMDB-12323, PDB-7nhc:
1918 H1N1 Viral influenza polymerase heterotrimer - Endonuclease ordered (Class2b)
Method: EM (single particle) / Resolution: 2.87 Å

EMDB-12342, PDB-7nhx:
1918 H1N1 Viral influenza polymerase heterotrimer - full transcriptase (Class1)
Method: EM (single particle) / Resolution: 3.23 Å

EMDB-12348, PDB-7ni0:
1918 H1N1 Viral influenza polymerase heterotrimer - Replicase (class 3)
Method: EM (single particle) / Resolution: 3.32 Å

EMDB-12361, PDB-7nik:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8189 core
Method: EM (single particle) / Resolution: 6.2 Å

EMDB-12362, PDB-7nil:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8190 core
Method: EM (single particle) / Resolution: 5.01 Å

EMDB-12363, PDB-7nir:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8191 core
Method: EM (single particle) / Resolution: 6.7 Å

EMDB-12364, PDB-7nis:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8192 core
Method: EM (single particle) / Resolution: 5.96 Å

EMDB-12371, PDB-7nj3:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8196 core
Method: EM (single particle) / Resolution: 4.48 Å

EMDB-12372, PDB-7nj4:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8198 core
Method: EM (single particle) / Resolution: 5.84 Å

EMDB-12373, PDB-7nj5:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8199 core
Method: EM (single particle) / Resolution: 4.63 Å

EMDB-12375, PDB-7nj7:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8200 core
Method: EM (single particle) / Resolution: 4.82 Å

EMDB-12428, PDB-7nk1:
1918 Influenza virus polymerase heterotirmer in complex with vRNA promoters and Nb8201
Method: EM (single particle) / Resolution: 4.22 Å

EMDB-12429, PDB-7nk2:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8202 core
Method: EM (single particle) / Resolution: 4.84 Å

EMDB-12430, PDB-7nk4:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8203 core
Method: EM (single particle) / Resolution: 5.32 Å

EMDB-12431, PDB-7nk6:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8204
Method: EM (single particle) / Resolution: 6.72 Å

EMDB-12433, PDB-7nk8:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8205 core
Method: EM (single particle) / Resolution: 5.34 Å

EMDB-12435, PDB-7nka:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8206
Method: EM (single particle) / Resolution: 4.07 Å

EMDB-12437, PDB-7nkc:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8207
Method: EM (single particle) / Resolution: 4.46 Å

EMDB-12440, PDB-7nki:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8209 core
Method: EM (single particle) / Resolution: 4.67 Å

EMDB-12447, PDB-7nkr:
1918 H1N1 Viral influenza polymerase heterotrimer with Nb8210
Method: EM (single particle) / Resolution: 5.6 Å

PDB-7nfq:
Fujian capmidlink domain in complex with Nb8193
Method: X-RAY DIFFRACTION / Resolution: 1.68 Å

PDB-7nfr:
Fujian capmidlink domain in complex with Nb8194
Method: X-RAY DIFFRACTION / Resolution: 1.88 Å

PDB-7nft:
Fujian capbinding domain in complex with Nb8208
Method: X-RAY DIFFRACTION / Resolution: 3.14 Å

Chemicals

ChemComp-GOL:
GLYCEROL / Glycerol

ChemComp-PEG:
DI(HYDROXYETHYL)ETHER / Diethylene glycol

ChemComp-HOH:
WATER / Water

ChemComp-SO4:
SULFATE ION / Sulfate

Source
  • influenza a virus (strain a/brevig mission/1/1918 h1n1)
  • synthetic construct (others)
  • staphylococcus aureus (bacteria)
  • influenza a virus (a/brevig mission/1/1918(h1n1))
  • camelidae mixed library (mammal)
  • Influenza A virus (A/Brevig Mission/1/1918(H1N1))
  • influenza a virus (a/duck/fujian/13/2002(h5n1))
  • homo sapiens (human)
KeywordsVIRAL PROTEIN / Influenza polymerase / cap-binding domain / nanobody / Influenza / RNA polymerase / H1N1 / 1918 / Influenza virus / polymerase / RdRp

+
About Yorodumi Papers

-
News

-
Feb 9, 2022. New format data for meta-information of EMDB entries

New format data for meta-information of EMDB entries

  • Version 3 of the EMDB header file is now the official format.
  • The previous official version 1.9 will be removed from the archive.

Related info.:EMDB header

External links:wwPDB to switch to version 3 of the EMDB data model

-
Aug 12, 2020. Covid-19 info

Covid-19 info

URL: https://pdbj.org/emnavi/covid19.php

New page: Covid-19 featured information page in EM Navigator.

Related info.:Covid-19 info / Mar 5, 2020. Novel coronavirus structure data

+
Mar 5, 2020. Novel coronavirus structure data

Novel coronavirus structure data

Related info.:Yorodumi Speices / Aug 12, 2020. Covid-19 info

External links:COVID-19 featured content - PDBj / Molecule of the Month (242):Coronavirus Proteases

+
Jan 31, 2019. EMDB accession codes are about to change! (news from PDBe EMDB page)

EMDB accession codes are about to change! (news from PDBe EMDB page)

  • The allocation of 4 digits for EMDB accession codes will soon come to an end. Whilst these codes will remain in use, new EMDB accession codes will include an additional digit and will expand incrementally as the available range of codes is exhausted. The current 4-digit format prefixed with “EMD-” (i.e. EMD-XXXX) will advance to a 5-digit format (i.e. EMD-XXXXX), and so on. It is currently estimated that the 4-digit codes will be depleted around Spring 2019, at which point the 5-digit format will come into force.
  • The EM Navigator/Yorodumi systems omit the EMD- prefix.

Related info.:Q: What is EMD? / ID/Accession-code notation in Yorodumi/EM Navigator

External links:EMDB Accession Codes are Changing Soon! / Contact to PDBj

+
Jul 12, 2017. Major update of PDB

Major update of PDB

  • wwPDB released updated PDB data conforming to the new PDBx/mmCIF dictionary.
  • This is a major update changing the version number from 4 to 5, and with Remediation, in which all the entries are updated.
  • In this update, many items about electron microscopy experimental information are reorganized (e.g. em_software).
  • Now, EM Navigator and Yorodumi are based on the updated data.

External links:wwPDB Remediation / Enriched Model Files Conforming to OneDep Data Standards Now Available in the PDB FTP Archive

-
Yorodumi Papers

Database of articles cited by EMDB/PDB/SASBDB data

  • Database of articles cited by EMDB, PDB, and SASBDB entries
  • Using PubMed data

Related info.:EMDB / PDB / SASBDB / Yorodumi / EMN Papers / Changes in new EM Navigator and Yorodumi

Read more