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InterPro: IPR014023 RNA-directed RNA polymerase catalytic

Protein matchesHelp
UniProtKB
Matches:
563 proteins
AccessionHelp IPR014023 RNA-dir_pol_cat
SecondaryHelp IPR007100
TypeHelp Domain
SignaturesHelp
InterPro RelationshipsHelp
Found in IPR001016 RNA-dependent RNA polymerase, L protein, viral
IPR016269 RNA-directed RNA polymerase, paramyxovirus
IPR017234 RNA-directed RNA polymerase, rhabdovirus
IPR017235 RNA-directed RNA polymerase, filovirus
GO Term annotationHelp
Process GO:0006370 mRNA capping
GO:0006410 transcription, RNA-dependent
Function GO:0003968 RNA-directed RNA polymerase activity
GO:0004482 mRNA (guanine-N7-)-methyltransferase activity
GO:0005524 ATP binding
Component GO:0005737 cytoplasm
GO:0019012 virion
InterPro annotation
BioMart Logo Entry Details in BioMart
AbstractHelp

RNA-directed RNA polymerase (RdRp) (EC:2.7.7.48) is an essential protein encoded in the genomes of all RNA containing viruses with no DNA stage [1, 2]. It catalyses synthesis of the RNA strand complementary to a given RNA template, but the precise molecular mechanism remains unclear. The postulated RNA replication process is a two-step mechanism. First, the initiation step of RNA synthesis begins at or near the 3' end of the RNA template by means of a primer-independent (de novo) mechanism. The de novo initiation consists in the addition of a nucleotide tri-phosphate (NTP) to the 3'-OH of the first initiating NTP. During the following so-called elongation phase, this nucleotidyl transfer reaction is repeated with subsequent NTPs to generate the complementary RNA product [3].

All the RNA-directed RNA polymerases, and many DNA-directed polymerases, employ a fold whose organisation has been likened to the shape of a right hand with three subdomains termed fingers, palm and thumb [4]. Only the palm subdomain, composed of a four-stranded antiparallel beta-sheet with two alpha-helices, is well conserved among all of these enzymes. In RdRp, the palm subdomain comprises three well conserved motifs (A, B and C). Motif A (D-x(4,5)-D) and motif C (GDD) are spatially juxtaposed; the Asp residues of these motifs are implied in the binding of Mg2+ and/or Mn2+. The Asn residue of motif B is involved in selection of ribonucleoside triphosphates over dNTPs and thus determines whether RNA is synthesised rather than DNA [5]. The domain organisation [6] and the 3D structure of the catalytic centre of a wide range of RdPp's, even those with a low overall sequence homology, are conserved. The catalytic centre is formed by several motifs containing a number of conserved amino acid residues.

There are 4 superfamilies of viruses that cover all RNA containing viruses with no DNA stage:

  • Viruses containing positive-strand RNA or double-strand RNA, except retroviruses and Birnaviridae: viral RNA-directed RNA polymerases including all positive-strand RNA viruses with no DNA stage, double-strand RNA viruses, and the Cystoviridae, Reoviridae, Hypoviridae, Partitiviridae, Totiviridae families.
  • Mononegavirales (negative-strand RNA viruses with non-segmented genomes).
  • Negative-strand RNA viruses with segmented genomes, i.e. Orthomyxoviruses (including influenza A, B, and C viruses, Thogotoviruses, and the infectious salmon anemia virus), Arenaviruses, Bunyaviruses, Hantaviruses, Nairoviruses, Phleboviruses, Tenuiviruses and Tospoviruses.
  • Birnaviridae family of dsRNA viruses.
The RNA-directed RNA polymerases in the first of the above superfamilies can be divided into the following three subgroups:
  • All positive-strand RNA eukaryotic viruses with no DNA stage.
  • All RNA-containing bacteriophages -there are two families of RNA-containing bacteriophages: Leviviridae (positive ssRNA phages) and Cystoviridae (dsRNA phages).
  • Reoviridae family of dsRNA viruses.

This entry represents the catalytic domain RNA-directed RNA polymerase.

Database linksHelp
PROSITE doc: PDOC50507

Taxonomic coverageHelp

Overlapping InterPro entriesHelp
IPR014023 Numbers of overlapping proteins Average numbers of overlapping amino acids

Example proteinsHelp
A3F5L9 Large structural protein

More proteins


Example Proteins Key


InterPro entry accession number/name and structure databases Colour code
IPR001016 RNA-dependent RNA polymerase, L protein, viral
IPR014023 RNA-directed RNA polymerase catalytic
IPR017234 RNA-directed RNA polymerase, rhabdovirus

PublicationsHelp
1. Koonin EV, Gorbalenya AE, Chumakov KM.
Tentative identification of RNA-dependent RNA polymerases of dsRNA viruses and their relationship to positive strand RNA viral polymerases.
FEBS Lett. 252 42-6 1989 [PubMed: 2759231]
http://dx.doi.org/10.1016/0014-5793(89)80886-5
2. Zanotto PM, Gibbs MJ, Gould EA, Holmes EC.
A reevaluation of the higher taxonomy of viruses based on RNA polymerases.
J. Virol. 70 6083-96 1996 [PubMed: 8709232]
http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=EBI&pubmedid=8709232
3. Kao CC, Singh P, Ecker DJ.
De novo initiation of viral RNA-dependent RNA synthesis.
Virology 287 251-60 2001 [PubMed: 11531403]
http://dx.doi.org/10.1006/viro.2001.1039
4. Hansen JL, Long AM, Schultz SC.
Structure of the RNA-dependent RNA polymerase of poliovirus.
Structure 5 1109-22 1997 [PubMed: 9309225]
http://dx.doi.org/10.1016/S0969-2126(97)00261-X
5. Gohara DW, Crotty S, Arnold JJ, Yoder JD, Andino R, Cameron CE.
Poliovirus RNA-dependent RNA polymerase (3Dpol): structural, biochemical, and biological analysis of conserved structural motifs A and B.
J. Biol. Chem. 275 25523-32 2000 [PubMed: 10827187]
http://dx.doi.org/10.1074/jbc.M002671200
6. O'Reilly EK, Kao CC.
Analysis of RNA-dependent RNA polymerase structure and function as guided by known polymerase structures and computer predictions of secondary structure.
Virology 252 287-303 1998 [PubMed: 9878607]
http://dx.doi.org/10.1006/viro.1998.9463

Additional ReadingHelp
Shwed PS, Dobos P, Cameron LA, Vakharia VN, Duncan R.
Birnavirus VP1 proteins form a distinct subgroup of RNA-dependent RNA polymerases lacking a GDD motif.
Virology 296 2002 241-50 [PubMed: 12069523]
http://dx.doi.org/10.1006/viro.2001.1334
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