Summary: Coronavirus RNA synthesis protein NSP10
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Coronavirus RNA synthesis protein NSP10 Provide feedback
Non-structural protein 10 (NSP10) is involved in RNA synthesis. It is synthesised as a polyprotein whose cleavage generates many non-structural proteins. NSP10 contains two zinc binding motifs and forms two anti-parallel helices which are stacked against an irregular beta sheet [1]. A cluster of basic residues on the protein surface suggests a nucleic acid-binding function. NSP10 interacts with NSP14 and NSP16 and regulates their respective ExoN and 2-O-MTase activities [2]. When binding to the N-terminal of NSP14, nsp10 allows the ExoN active site to adopt a stably closed conformation [3] and is an allosteric regulator that stabilizes NSP16. The residue Tyr-96 plays a crucial role in the NSP10-NSP16/NSP14 interaction. This residue is specific for SARS-CoV NSP10 and is a phenylalanine in most other Coronavirus homologues [4].
Literature references
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Joseph JS, Saikatendu KS, Subramanian V, Neuman BW, Brooun A, Griffith M, Moy K, Yadav MK, Velasquez J, Buchmeier MJ, Stevens RC, Kuhn P; , J Virol. 2006;80:7894-7901.: Crystal structure of nonstructural protein 10 from the severe acute respiratory syndrome coronavirus reveals a novel fold with two zinc-binding motifs. PUBMED:16873246 EPMC:16873246
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Snijder EJ, Decroly E, Ziebuhr J;, Adv Virus Res. 2016;96:59-126.: The Nonstructural Proteins Directing Coronavirus RNA Synthesis and Processing. PUBMED:27712628 EPMC:27712628
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Ferron F, Subissi L, Silveira De Morais AT, Le NTT, Sevajol M, Gluais L, Decroly E, Vonrhein C, Bricogne G, Canard B, Imbert I;, Proc Natl Acad Sci U S A. 2018;115:E162.: Structural and molecular basis of mismatch correction and ribavirin excision from coronavirus RNA. PUBMED:29279395 EPMC:29279395
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Bouvet M, Lugari A, Posthuma CC, Zevenhoven JC, Bernard S, Betzi S, Imbert I, Canard B, Guillemot JC, Lecine P, Pfefferle S, Drosten C, Snijder EJ, Decroly E, Morelli X;, J Biol Chem. 2014;289:25783-25796.: Coronavirus Nsp10, a critical co-factor for activation of multiple replicative enzymes. PUBMED:25074927 EPMC:25074927
This tab holds annotation information from the InterPro database.
InterPro entry IPR018995
Non-structural protein 10 (NSP10) is involved in RNA synthesis. It is synthesised as part of a replicase polyprotein, whose cleavage generates many non-structural proteins [PUBMED:17634238]. NSP10 contains two zinc binding motifs and forms two anti-parallel helices which are stacked against an irregular beta sheet [PUBMED:16873246]. A cluster of basic residues on the protein surface suggests a nucleic acid-binding function.
Gene Ontology
The mapping between Pfam and Gene Ontology is provided by InterPro. If you use this data please cite InterPro.
Molecular function | RNA binding (GO:0003723) |
zinc ion binding (GO:0008270) | |
Biological process | viral genome replication (GO:0019079) |
Domain organisation
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Alignments
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Seed (6) |
Full (127) |
Representative proteomes | UniProt (3011) |
NCBI (3150) |
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RP15 (124) |
RP35 (124) |
RP55 (124) |
RP75 (124) |
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PP/heatmap | 1 |
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
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Seed (6) |
Full (127) |
Representative proteomes | UniProt (3011) |
NCBI (3150) |
Meta (0) |
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RP15 (124) |
RP35 (124) |
RP55 (124) |
RP75 (124) |
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Gzipped |
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
HMM logo
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Trees
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Curation and family details
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Curation
Seed source: | pdb_2fyg |
Previous IDs: | NSP10; nsp10; |
Type: | Family |
Sequence Ontology: | SO:0100021 |
Author: |
Mistry J |
Number in seed: | 6 |
Number in full: | 127 |
Average length of the domain: | 122.20 aa |
Average identity of full alignment: | 58 % |
Average coverage of the sequence by the domain: | 2.10 % |
HMM information
HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 47079205 -E 1000 --cpu 4 HMM pfamseq
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Model details: |
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Model length: | 122 | ||||||||||||
Family (HMM) version: | 11 | ||||||||||||
Download: | download the raw HMM for this family |
Species distribution
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Interactions
Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the CoV_NSP10 domain has been found. There are 75 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein sequence.
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