Coronavirus (CoV) proteins | Other protein targets | IUPHAR/BPS Guide to PHARMACOLOGY

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Coronavirus (CoV) proteins C

Overview

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Coronaviruses are large, often spherical, enveloped, single-stranded positive-sense RNA viruses, ranging in size from 80-220 nm. Their genomes and protein structures are highly conserved. Three coronaviruses have emerged over the last 20 years as serious human pathogens: SARS-CoV was identified as the causative agent in an outbreak in 2002-2003, Middle East respiratory syndrome (MERS) CoV emerged in 2012 and the novel coronavirus SARS-CoV-2 emerged in 2019-2020. SARS-CoV-2 is the virus responsible for the infectious disease termed COVID-19 (WHO Technical Guidance 2020).

Targets

Complexes

CoV 2'-O-methyltransferase Show summary »« Hide summary More detailed page go icon to follow link

Target Id

3277

Nomenclature

CoV 2'-O-methyltransferase

Previous and unofficial names

RNA 2′-O-MTase

Subunits

CoV Non-structural protein 10
CoV Non-structural protein 16
The coronavirus nsp10 and nsp16 proteins form an enzymatically active heterodimer with 2'-O-methyltransferase activity.

Inhibitors

sinefungin pIC₅₀ 5.5 [14] - SARS-CoV-2

nsp16 inhibitor 5a pIC₅₀ 5.1 [13] - SARS-CoV-2

Comment

The betacoronavirus replicase encodes non-structural proteins that catalyse methylation of the viral mRNA: nsp14 behaves as a N⁷-MTase to generate the N⁷mGppp-RNA (Cap-0) structure (this improves viral protein translation), and nsp16 is a 2′-O-MTase (EC 2.1.1.57) that creates the N⁷mGpppA-2′-O-Me (Cap-1) structure. RNA capping also acts to protect the RNAs from degradation and to limit host immune detection.
Nsp16 forms a functional heterodimeric complex with nsp10. 2'-O-methyltransferase inhibitors are of interest as potential pan-coronavirus therapeutics [8,13]

Targets and Subunits

CoV Envelope protein Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3116
Nomenclature	CoV Envelope protein
Previous and unofficial names	envelope small membrane protein \| orf4
UniProtKB AC	P0DTC4 (SARS-CoV-2), P59637 (SARS-CoV)
Comment	By similarity to other coronavirus E proteins, SARS-CoV-2 E is predicted to constitute a single transmembrane (potentially homopentameric) ion channel with selectivity for monovalent cations over monovalent anions [24,33,39,43]. E increases the intracellular Cl^- concentration in airway epithelial cells, which disrupts airway epithelial barrier function and aggravates airway inflammation during SARS-CoV-2 infection [41].

CoV 3C-like (main) protease C Show summary »« Hide summary More detailed page go icon to follow link

Target Id

3111

Nomenclature

CoV 3C-like (main) protease

Previous and unofficial names

UniProtKB AC

P0C6U8 (SARS-CoV)

EC number (SARS-CoV-2)

3.4.22.69

Inhibitors

nirmatrelvir pK_i 9.6 [23] - SARS-CoV-2

bofutrelvir pIC₅₀ 7.3 [3] - SARS-CoV-2

Comment

The Mpro enzyme (also known as nsp5 or 3CL protease) cleaves the two polyproteins encoded by the SARS-CoV-2 genome (pp1a and pp1ab) into a range of non-structural proteins (nsp1-11 from pp1a; nsp1-16 from pp1ab). As these component proteins play crucial roles in viral replication, Mpro is considered to be a strong molecular target for drug development. Small molecule Mpro inhibitors would be predicted to reduce viral replication [11,18,27].

CoV Membrane glycoprotein Show summary »« Hide summary More detailed page go icon to follow link

Target Id

3117

Nomenclature

CoV Membrane glycoprotein

Previous and unofficial names

membrane protein

UniProtKB AC

P0DTC5 (SARS-CoV-2), P59596 (SARS-CoV)

Inhibitors

JNJ-9676 [36] - SARS-CoV-2

Comment

The membrane glycoprotein (M) is usually regarded as the most abundant protein in the coronavirus envelope. By similarity with other coronavirus M proteins it is predicted to be essential for initiating assembly of the viral envelope components [29,44].

CoV Non-structural protein 6 Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3118
Nomenclature	CoV Non-structural protein 6
Previous and unofficial names	nsp6
UniProtKB AC	P0DTC6 (SARS-CoV-2), P59634 (SARS-CoV)
Comment	Coronavirus nsp6 proteins limit autophagosome expansion [2]. This mechanism may favour coronavirus infection by damaging autophagosome-mediated delivery of viral components to lysosomes for degradation.

CoV Non-structural protein 7b Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3123
Nomenclature	CoV Non-structural protein 7b
Previous and unofficial names	Accessory protein 7b \| nsp7b
UniProtKB AC	P0DTD8 (SARS-CoV-2), Q7TFA1 (SARS-CoV)
Comment	Protein 7b is a coronavirus accessory protein. Experimental evidence suggests that SARS-CoV 7b has some attenuating function [26]. By homology, SARS-CoV-2 7b is likely to have a similar function.

CoV Non-structural protein 8 Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3120
Nomenclature	CoV Non-structural protein 8
Previous and unofficial names	nsp8
UniProtKB AC	P0DTC8 (SARS-CoV-2)
Comment	Coronavirus nsp8 proteins form a hexadecameric complex with nsp7 proteins (8 subunits of each) [12,35]. This complex may participate in viral replication by acting as a primase for de novo initiation of RNA synthesis.

CoV Non-structural protein 10 Show summary »« Hide summary

Target Id	3275
Nomenclature	CoV Non-structural protein 10
Previous and unofficial names	Nsp10
Complexes	CoV 2'-O-methyltransferase
UniProtKB AC	P0DTC8 (SARS-CoV-2)
Comment	Nsp10 is a subunit of the betacoronavirus 2'-O-methyltransferase (EC 2.1.1.57) heterodimer with nsp16. 2′-O-MTase-catalysed methlyation creates the N⁷mGpppA-2′-O-Me (Cap-1) structure on viral mRNA transcripts. Evidence suggests that nsp10 interacts with nsp14 to form a complex with proofreading exonuclease activity [28]. Inhibiting nsp14's exonuclease activity offers an additional mechanism to achieve broad-spectrum anti-coronavirus therapeutic potential.

CoV Non-structural protein 13 Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3261
Nomenclature	CoV Non-structural protein 13
UniProtKB AC	P0DTD1 (SARS-CoV-2)
Comment	Nsp13 is a helicase that is encoded by coronavirus (CoV) RNAs. The SARS-CoV-2 nsp13 is 600 aa long. Small molecule nsp13 inhibitors are proposed as novel CoV antivirals.

CoV Non-structural protein 14 Show summary »« Hide summary More detailed page go icon to follow link

Target Id

3198

Nomenclature

CoV Non-structural protein 14

Previous and unofficial names

(N7-guanine)-methyltransferase | N7-MTase

UniProtKB AC

P0DTD8 (SARS-CoV-2), P59634 (SARS-CoV)

Inhibitors

NSC620333 pK_d 6.4 [20] - SARS-CoV-2

TO507 pIC₅₀ 8.5 [22] - SARS-CoV-2

CoV Non-structural protein 15 C Show summary »« Hide summary More detailed page go icon to follow link

Target Id

3206

Nomenclature

CoV Non-structural protein 15

Previous and unofficial names

NendoU | NSP15

UniProtKB AC

P0DTD1 (SARS-CoV-2), P0C6X7 (SARS-CoV)

Inhibitors

tipiracil [16] - SARS-CoV-2

Comment

Nsp15 (NendoU) is a uridylate-specific endoribonuclease that is essential during the coronavirus lifecycle. The search for inhibitors of SARS-CoV-2 nsp15 that may have antiviral action is ongoing. Two allosteric inhibitors have been reported, FUZS-5 (12200) and LIZA-7 (12199). The docking positions of these compounds within nsp15 have been determined by X-ray crystallography [6].

CoV Non-structural protein 16 Show summary »« Hide summary

Target Id

3276

Nomenclature

CoV Non-structural protein 16

Previous and unofficial names

Nsp16

Complexes

CoV 2'-O-methyltransferase

UniProtKB AC

P0DTC8 (SARS-CoV-2)

Inhibitors

CoV nsp16 inhibitor 2a [PMID: 34257831] pIC₅₀ 8.4 [1] - SARS-CoV-2

sinefungin pIC₅₀ 6.1 [17] - SARS-CoV

SS148 pIC₅₀ 6.0 [19] - SARS-CoV

SS148 pIC₅₀ 6.0 [19], 5.9 [19] - SARS-CoV-2

SS148 pIC₅₀ 5.8 [19] - MERS-CoV

Comment

Nsp16 is a subunit of the betacoronavirus 2'-O-methyltransferase (mRNA capping enzyme). Heterodimerisation with nsp10 is required for activation of nsp16's 2'-O-MTase function [37]. The activated enzyme generates the N⁷mGpppA-2′-O-Me (Cap-1) structure on viral mRNA transcripts.

CoV Nucleoprotein Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3121
Nomenclature	CoV Nucleoprotein
Previous and unofficial names	nucleocapsid phosphoprotein
UniProtKB AC	P0DTC9 (SARS-CoV-2), P59595 (SARS-CoV)
Comment	The coronavirus nucleocapsid phosphoprotein (N, or nucleoprotein) is highly basic and binds the viral RNA as a dimeric entity [4] into nucleocapsids which protect the viral genome, while also providing access for replication when required.

CoV Papain-like protease C Show summary »« Hide summary More detailed page go icon to follow link

Target Id

3132

Nomenclature

CoV Papain-like protease

Previous and unofficial names

non-structural protein 3 | NS3 | nsp3 | PL-PRO

UniProtKB AC

P0DTC1 (SARS-CoV-2)

EC number (SARS-CoV-2)

3.4.22.46

Inhibitors

XR8-23 pIC₅₀ 6.4 [30] - SARS-CoV-2

GRL-0617 pIC₅₀ 5.6 – 5.6 [5,21] - SARS-CoV-2

Comment

PL-pro is a domain within coronavirus Nsp3. Its proteolytic activity cleaves three sites in the viral replicase polyprotein (recognition consensus sequence LXGG↓XX) to release the three non-structural proteins Nsp1, Nsp2, and Nsp3 [10]. It has additional non-proteolytic functions as part of the multicomponent replicase-transcriptase complex [32].

CoV Protein 3a Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3115
Nomenclature	CoV Protein 3a
Previous and unofficial names	orf3a
UniProtKB AC	P0DTC3 (SARS-CoV-2), P59632 (SARS-CoV)
Comment	Protein 3a is a transmembrane pore-forming viral protein (viroporin) with potassium ion channel activity.

CoV Protein 7a Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3119
Nomenclature	CoV Protein 7a
Previous and unofficial names	orf7a
UniProtKB AC	P0DTC7 (SARS-CoV-2), P59635 (SARS-CoV)
Comment	The main function of the SARS-CoV protein 7a appears to be disruption of host the cell cycle and induction of caspase-dependent apoptosis [34]. By homology SARS-CoV-2 protein 7a is likely to produce the same effect.

CoV Protein 9b Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3122
Nomenclature	CoV Protein 9b
Previous and unofficial names	orf9b \| Accessory protein 9b \| ORF-9b
UniProtKB AC	P0DTD2 (SARS-CoV-2), P59636 (SARS-CoV)
Comment	SARS-CoV protein 9b is a virion-associated accessory protein [42] that acts to block the host's ability to mount an antiviral IFN-induced innate immune response [31]. By homology, 9b from SARS-CoV-2 would be predicted to exhibit a similar function.

CoV Replicase polyprotein 1a Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3124
Nomenclature	CoV Replicase polyprotein 1a
UniProtKB AC	P0DTC1 (SARS-CoV-2), P0C6U8 (SARS-CoV)
Comment	The replicase polyprotein 1a (pp1a) encodes a set of 11 smaller proteins, including two proteases that are responsible for cleaving the polyprotein chain into its component parts. The components are non-structural and are involved in the transcription and replication of viral proteins and RNA.

CoV Replicase polyprotein 1ab Show summary »« Hide summary More detailed page go icon to follow link

Target Id	3125
Nomenclature	CoV Replicase polyprotein 1ab
UniProtKB AC	P0DTD1 (SARS-CoV-2), P0C6X7 (SARS-CoV)
Comment	The replicase polyprotein 1ab (pp1ab) encodes a set of 15 smaller proteins (5 more than pp1a), including two proteases that are responsible for cleaving the polyprotein chain into its component parts. The components are non-structural and are involved in the transcription and replication of viral proteins and RNA.

CoV RNA-dependent RNA polymerase C Show summary »« Hide summary More detailed page go icon to follow link

Target Id

3139

Nomenclature

CoV RNA-dependent RNA polymerase

Previous and unofficial names

non-structural protein 12 | nsp12

UniProtKB AC

P0DTD1 (SARS-CoV-2), P0C6X7 (SARS-CoV)

Inhibitors

remdesivir [7] - SARS-CoV-2

remdesivir [7] - SARS-CoV

Comment

The conservation of RdRP catalytic domain between different RNA viruses endows inhibitors that were designed against other viral pathogens with activity against the SARS coronaviruses. Viral RdRP is the molecular target of nucleotide-based broad-spectrum antiviral compounds like remdesivir, tenofovir and ribavirin [7,38,45].

CoV Spike glycoprotein C Show summary »« Hide summary More detailed page go icon to follow link

Target Id

3114

Nomenclature

CoV Spike glycoprotein

Previous and unofficial names

spike protein

UniProtKB AC

P0DTC2 (SARS-CoV-2), P59594 (SARS-CoV)

Inhibitors

EK-1-C4 (Binding) [40] - SARS-CoV-2

Antibodies

regdanvimab (Binding) pK_d 10.6 [15] - SARS-CoV-2

casirivimab (Binding) pIC₅₀ 10.2 [9] - SARS-CoV-2

Comment

The spike protein on the surface of CoV particles is central for viral infection of host cells (by binding to ACE2). It is the molecular target of a wide range of clinically approved monoclonal antibodies that reduce infection. At any point in time, the efficacy of these therapeutics is heavily dependent upon spike mutations in the circulating CoV variants. Spike is also the antigen that's exploited for raising anti-CoV immunity by inoculation with either mRNA and/or adenovirus vaccines that induce spike protein expression.

Comments

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References

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1. Bobiļeva O, Bobrovs R, Kaņepe I, Patetko L, Kalniņš G, Šišovs M, Bula AL, Gri Nberga S, Borodušķis MR, Ramata-Stunda A et al.. (2021) Potent SARS-CoV-2 mRNA Cap Methyltransferase Inhibitors by Bioisosteric Replacement of Methionine in SAM Cosubstrate. ACS Med Chem Lett, 12 (7): 1102-1107. [PMID:34257831]

2. Cottam EM, Whelband MC, Wileman T. (2014) Coronavirus NSP6 restricts autophagosome expansion. Autophagy, 10 (8): 1426-41. [PMID:24991833]

3. Dai W, Zhang B, Jiang XM, Su H, Li J, Zhao Y, Xie X, Jin Z, Peng J, Liu F et al.. (2020) Structure-based design of antiviral drug candidates targeting the SARS-CoV-2 main protease. Science, 368 (6497): 1331-1335. [PMID:32321856]

4. Fan H, Ooi A, Tan YW, Wang S, Fang S, Liu DX, Lescar J. (2005) The nucleocapsid protein of coronavirus infectious bronchitis virus: crystal structure of its N-terminal domain and multimerization properties. Structure, 13 (12): 1859-68. [PMID:16338414]

5. Freitas BT, Durie IA, Murray J, Longo JE, Miller HC, Crich D, Hogan RJ, Tripp RA, Pegan SD. (2020) Characterization and Noncovalent Inhibition of the Deubiquitinase and deISGylase Activity of SARS-CoV-2 Papain-Like Protease. ACS Infect Dis, 6 (8): 2099-2109. [PMID:32428392]

6. Godoy AS, Nakamura AM, Douangamath A, Song Y, Noske GD, Gawriljuk VO, Fernandes RS, Pereira HDM, Oliveira KIZ, Fearon D et al.. (2023) Allosteric regulation and crystallographic fragment screening of SARS-CoV-2 NSP15 endoribonuclease. Nucleic Acids Res, 51 (10): 5255-5270. DOI: 10.1101/2022.09.26.509485 [PMID:37115000]

7. Gordon CJ, Tchesnokov EP, Woolner E, Perry JK, Feng JY, Porter DP, Götte M. (2020) Remdesivir is a direct-acting antiviral that inhibits RNA-dependent RNA polymerase from severe acute respiratory syndrome coronavirus 2 with high potency. J Biol Chem, 295 (20): 6785-6797. [PMID:32284326]

8. Hanna GS, Benjamin MM, Choo YM, De R, Schinazi RF, Nielson SE, Hevel JM, Hamann MT. (2024) Informatics and Computational Approaches for the Discovery and Optimization of Natural Product-Inspired Inhibitors of the SARS-CoV-2 2'-O-Methyltransferase. J Nat Prod, 87 (2): 217-227. [PMID:38242544]

9. Hansen J, Baum A, Pascal KE, Russo V, Giordano S, Wloga E, Fulton BO, Yan Y, Koon K, Patel K et al.. (2020) Studies in humanized mice and convalescent humans yield a SARS-CoV-2 antibody cocktail. Science, 369 (6506): 1010-1014. [PMID:32540901]

10. Harcourt BH, Jukneliene D, Kanjanahaluethai A, Bechill J, Severson KM, Smith CM, Rota PA, Baker SC. (2004) Identification of severe acute respiratory syndrome coronavirus replicase products and characterization of papain-like protease activity. J Virol, 78 (24): 13600-12. [PMID:15564471]

11. Hilgenfeld R. (2014) From SARS to MERS: crystallographic studies on coronaviral proteases enable antiviral drug design. FEBS J, 281 (18): 4085-96. [PMID:25039866]

12. Imbert I, Guillemot JC, Bourhis JM, Bussetta C, Coutard B, Egloff MP, Ferron F, Gorbalenya AE, Canard B. (2006) A second, non-canonical RNA-dependent RNA polymerase in SARS coronavirus. EMBO J, 25 (20): 4933-42. [PMID:17024178]

13. Inniss NL, Kozic J, Li F, Rosas-Lemus M, Minasov G, Rybáček J, Zhu Y, Pohl R, Shuvalova L, Rulíšek L et al.. (2023) Discovery of a Druggable, Cryptic Pocket in SARS-CoV-2 nsp16 Using Allosteric Inhibitors. ACS Infect Dis, 9 (10): 1918-1931. [PMID:37728236]

14. Khalili Yazdi A, Li F, Devkota K, Perveen S, Ghiabi P, Hajian T, Bolotokova A, Vedadi M. (2021) A High-Throughput Radioactivity-Based Assay for Screening SARS-CoV-2 nsp10-nsp16 Complex. SLAS Discov, 26 (6): 757-765. [PMID:33874769]

15. Kim C, Ryu DK, Lee J, Kim YI, Seo JM, Kim YG, Jeong JH, Kim M, Kim JI, Kim P et al.. (2021) A therapeutic neutralizing antibody targeting receptor binding domain of SARS-CoV-2 spike protein. Nat Commun, 12 (1): 288. [PMID:33436577]

16. Kim Y, Wower J, Maltseva N, Chang C, Jedrzejczak R, Wilamowski M, Kang S, Nicolaescu V, Randall G, Michalska K et al.. (2021) Tipiracil binds to uridine site and inhibits Nsp15 endoribonuclease NendoU from SARS-CoV-2. Commun Biol, 4 (1): 193. [PMID:33564093]

17. Krafcikova P, Silhan J, Nencka R, Boura E. (2020) Structural analysis of the SARS-CoV-2 methyltransferase complex involved in RNA cap creation bound to sinefungin. Nat Commun, 11 (1): 3717. [PMID:32709887]

18. La Monica G, Bono A, Lauria A, Martorana A. (2022) Targeting SARS-CoV-2 Main Protease for Treatment of COVID-19: Covalent Inhibitors Structure-Activity Relationship Insights and Evolution Perspectives. J Med Chem, 65 (19): 12500-12534. [PMID:36169610]

19. Li F, Ghiabi P, Hajian T, Klima M, Li ASM, Khalili Yazdi A, Chau I, Loppnau P, Kutera M, Seitova A et al.. (2023) SS148 and WZ16 inhibit the activities of nsp10-nsp16 complexes from all seven human pathogenic coronaviruses. Biochim Biophys Acta Gen Subj, 1867 (4): 130319. [PMID:36764586]

20. Nigam AK, Hurley MFD, Fengling Li F, Konkoľová E, Klíma M, Trylčová J, Pollice R, Çinaroǧlu SS, Levin-Konigsberg R, Handjaya J et al.. (2024) Application of established computational techniques to identify potential SARS-CoV-2 Nsp14-MTase inhibitors in low data regimes. Digital Discovery, 3 (7): 1327-1341. DOI: 10.1039/D4DD00006D

21. Osipiuk J, Azizi SA, Dvorkin S, Endres M, Jedrzejczak R, Jones KA, Kang S, Kathayat RS, Kim Y, Lisnyak VG et al.. (2021) Structure of papain-like protease from SARS-CoV-2 and its complexes with non-covalent inhibitors. Nat Commun, 12 (1): 743. [PMID:33531496]

22. Otava T, Šála M, Li F, Fanfrlík J, Devkota K, Perveen S, Chau I, Pakarian P, Hobza P, Vedadi M et al.. (2021) The Structure-Based Design of SARS-CoV-2 nsp14 Methyltransferase Ligands Yields Nanomolar Inhibitors. ACS Infect Dis, 7 (8): 2214-2220. [PMID:34152728]

23. Owen DR, Allerton CMN, Anderson AS, Aschenbrenner L, Avery M, Berritt S, Boras B, Cardin RD, Carlo A, Coffman KJ et al.. (2021) An oral SARS-CoV-2 M^pro inhibitor clinical candidate for the treatment of COVID-19. Science, 374 (6575): 1586-1593. [PMID:34726479]

24. Pervushin K, Tan E, Parthasarathy K, Lin X, Jiang FL, Yu D, Vararattanavech A, Soong TW, Liu DX, Torres J. (2009) Structure and inhibition of the SARS coronavirus envelope protein ion channel. PLoS Pathog, 5 (7): e1000511. [PMID:19593379]

25. Petersen E, Koopmans M, Go U, Hamer DH, Petrosillo N, Castelli F, Storgaard M, Al Khalili S, Simonsen L. (2020) Comparing SARS-CoV-2 with SARS-CoV and influenza pandemics. Lancet Infect Dis, 20 (9): e238-e244. [PMID:32628905]

26. Pfefferle S, Krähling V, Ditt V, Grywna K, Mühlberger E, Drosten C. (2009) Reverse genetic characterization of the natural genomic deletion in SARS-Coronavirus strain Frankfurt-1 open reading frame 7b reveals an attenuating function of the 7b protein in-vitro and in-vivo. Virol J, 6: 131. [PMID:19698190]

27. Pillaiyar T, Manickam M, Namasivayam V, Hayashi Y, Jung SH. (2016) An Overview of Severe Acute Respiratory Syndrome-Coronavirus (SARS-CoV) 3CL Protease Inhibitors: Peptidomimetics and Small Molecule Chemotherapy. J Med Chem, 59 (14): 6595-628. [PMID:26878082]

28. Rona G, Zeke A, Miwatani-Minter B, de Vries M, Kaur R, Schinlever A, Garcia SF, Goldberg HV, Wang H, Hinds TR et al.. (2022) The NSP14/NSP10 RNA repair complex as a Pan-coronavirus therapeutic target. Cell Death Differ, 29 (2): 285-292. [PMID:34862481]

29. Ruch TR, Machamer CE. (2012) The coronavirus E protein: assembly and beyond. Viruses, 4 (3): 363-82. [PMID:22590676]

30. Shen Z, Ratia K, Cooper L, Kong D, Lee H, Kwon Y, Li Y, Alqarni S, Huang F, Dubrovskyi O et al.. (2022) Design of SARS-CoV-2 PLpro Inhibitors for COVID-19 Antiviral Therapy Leveraging Binding Cooperativity. J Med Chem, 65 (4): 2940-2955. [PMID:34665619]

31. Shi CS, Qi HY, Boularan C, Huang NN, Abu-Asab M, Shelhamer JH, Kehrl JH. (2014) SARS-coronavirus open reading frame-9b suppresses innate immunity by targeting mitochondria and the MAVS/TRAF3/TRAF6 signalosome. J Immunol, 193 (6): 3080-9. [PMID:25135833]

32. Shin D, Mukherjee R, Grewe D, Bojkova D, Baek K, Bhattacharya A, Schulz L, Widera M, Mehdipour AR, Tascher G et al.. (2020) Papain-like protease regulates SARS-CoV-2 viral spread and innate immunity. Nature, 587 (7835): 657-662. [PMID:32726803]

33. Surya W, Li Y, Verdià-Bàguena C, Aguilella VM, Torres J. (2015) MERS coronavirus envelope protein has a single transmembrane domain that forms pentameric ion channels. Virus Res, 201: 61-6. [PMID:25733052]

34. Tan YJ, Fielding BC, Goh PY, Shen S, Tan TH, Lim SG, Hong W. (2004) Overexpression of 7a, a protein specifically encoded by the severe acute respiratory syndrome coronavirus, induces apoptosis via a caspase-dependent pathway. J Virol, 78 (24): 14043-7. [PMID:15564512]

35. te Velthuis AJ, van den Worm SH, Snijder EJ. (2012) The SARS-coronavirus nsp7+nsp8 complex is a unique multimeric RNA polymerase capable of both de novo initiation and primer extension. Nucleic Acids Res, 40 (4): 1737-47. [PMID:22039154]

36. Van Damme E, Abeywickrema P, Yin Y, Xie J, Jacobs S, Mann MK, Doijen J, Miller R, Piassek M, Marsili S et al.. (2025) A small-molecule SARS-CoV-2 inhibitor targeting the membrane protein. Nature, [Epub ahead of print]. [PMID:40140563]

37. Vithani N, Ward MD, Zimmerman MI, Novak B, Borowsky JH, Singh S, Bowman GR. (2021) SARS-CoV-2 Nsp16 activation mechanism and a cryptic pocket with pan-coronavirus antiviral potential. Biophys J, 120 (14): 2880-2889. [PMID:33794150]

38. Wang Y, Anirudhan V, Du R, Cui Q, Rong L. (2021) RNA-dependent RNA polymerase of SARS-CoV-2 as a therapeutic target. J Med Virol, 93 (1): 300-310. [PMID:32633831]

39. Wilson L, McKinlay C, Gage P, Ewart G. (2004) SARS coronavirus E protein forms cation-selective ion channels. Virology, 330 (1): 322-31. [PMID:15527857]

40. Xia S, Liu M, Wang C, Xu W, Lan Q, Feng S, Qi F, Bao L, Du L, Liu S et al.. (2020) Inhibition of SARS-CoV-2 (previously 2019-nCoV) infection by a highly potent pan-coronavirus fusion inhibitor targeting its spike protein that harbors a high capacity to mediate membrane fusion. Cell Res, 30 (4): 343-355. [PMID:32231345]

41. Xu JB, Guan WJ, Zhang YL, Qiu ZE, Chen L, Hou XC, Yue J, Zhou YY, Sheng J, Zhao L et al.. (2024) SARS-CoV-2 envelope protein impairs airway epithelial barrier function and exacerbates airway inflammation via increased intracellular Cl^- concentration. Signal Transduct Target Ther, 9 (1): 74. [PMID:38528022]

42. Xu K, Zheng BJ, Zeng R, Lu W, Lin YP, Xue L, Li L, Yang LL, Xu C, Dai J et al.. (2009) Severe acute respiratory syndrome coronavirus accessory protein 9b is a virion-associated protein. Virology, 388 (2): 279-85. [PMID:19394665]

43. Zhang R, Wang K, Lv W, Yu W, Xie S, Xu K, Schwarz W, Xiong S, Sun B. (2014) The ORF4a protein of human coronavirus 229E functions as a viroporin that regulates viral production. Biochim Biophys Acta, 1838 (4): 1088-95. [PMID:23906728]

44. Zhang Z, Nomura N, Muramoto Y, Ekimoto T, Uemura T, Liu K, Yui M, Kono N, Aoki J, Ikeguchi M et al.. (2022) Structure of SARS-CoV-2 membrane protein essential for virus assembly. Nat Commun, 13 (1): 4399. [PMID:35931673]

45. Zhu W, Chen CZ, Gorshkov K, Xu M, Lo DC, Zheng W. (2020) RNA-Dependent RNA Polymerase as a Target for COVID-19 Drug Discovery. SLAS Discov, 25 (10): 1141-1151. [PMID:32660307]

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Concise Guide to PHARMACOLOGY citation:

Alexander SPH, Kelly E, Mathie AA, Peters JA, Veale EL, Armstrong JF, Buneman OP, Faccenda E, Harding SD, Spedding M, Cidlowski JA, Fabbro D, Davenport AP, Striessnig J, Davies JA et al. (2023) The Concise Guide to PHARMACOLOGY 2023/24: Introduction and Other Protein Targets. Br J Pharmacol. 180 Suppl 2:S1-22.