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. 2017 Sep 1:149–158. doi: 10.1016/B978-0-12-803109-4.00017-9

Table 17.1.

Coronavirus nsps That form the Replicase/Transcriptase Complex*

Nonstructural protein Function
nsp1 Interferon antagonist (not present in all coronaviruses)
nsp2 Not known
nsp3 Papain-like protease domains and several other protein interaction domains. May tether the RNA genome to the replicase/transcriptase complex.
nsp4 Transmembrane scaffold. Involved in membrane remodeling.
nsp5 Main protease (Mpro) (also called 3C-like protease)
nsp6 Transmembrane scaffold. Involved in membrane remodeling.
nsp7 Forms a large complex with nsp8.
nsp8 Forms a large complex with nsp7. The complex may function as a processivity clamp for the RdRp.
nsp9 Single-stranded RNA-binding protein
nsp10 Zinc-binding cofactor for 2′-O-methyltransferase (nsp16)
nsp12 RdRp
nsp13 RNA 5′ triphosphatase (cap synthesis), RNA helicase
nsp14 N7-methyltransferase, Exo N 3′–5′ exonuclease (provides a proofreading function for the coronavirus RdRp)
nsp15 Nendo U endonuclease (cleaves single- and double-stranded RNA downstream of uridylate residues, producing 2–3 cyclic phosphates).
nsp16 2′-O-methyltransferase (cap synthesis)

*Products of polyproteins 1a and 1b.