Viral replicase gene products suffice for coronavirus discontinuous transcription.
about
The footprint of genome architecture in the largest genome expansion in RNA virusesReverse genetics system for the avian coronavirus infectious bronchitis virusCoronavirus reverse genetic systems: infectious clones and repliconsA second, non-canonical RNA-dependent RNA polymerase in SARS CoronavirusNovel β-Barrel Fold in the Nuclear Magnetic Resonance Structure of the Replicase Nonstructural Protein 1 from the Severe Acute Respiratory Syndrome CoronavirusThe crystal structures of severe acute respiratory syndrome virus main protease and its complex with an inhibitorNuclear Magnetic Resonance Structure Shows that the Severe Acute Respiratory Syndrome Coronavirus-Unique Domain Contains a Macrodomain FoldDiscovery, synthesis, and structure-based optimization of a series of N-(tert-butyl)-2-(N-arylamido)-2-(pyridin-3-yl) acetamides (ML188) as potent noncovalent small molecule inhibitors of the severe acute respiratory syndrome coronavirus (SARS-CoV)Targeting zoonotic viruses: Structure-based inhibition of the 3C-like protease from bat coronavirus HKU4--The likely reservoir host to the human coronavirus that causes Middle East Respiratory Syndrome (MERS)Anti-SARS coronavirus agents: a patent review (2008 - present).Coronavirus nucleocapsid protein facilitates template switching and is required for efficient transcriptionSelective replication of coronavirus genomes that express nucleocapsid proteinAchieving a golden mean: mechanisms by which coronaviruses ensure synthesis of the correct stoichiometric ratios of viral proteins.The coronavirus nucleocapsid is a multifunctional protein.An interaction between the nucleocapsid protein and a component of the replicase-transcriptase complex is crucial for the infectivity of coronavirus genomic RNA.Antiviral drugs specific for coronaviruses in preclinical developmentRNA replication of mouse hepatitis virus takes place at double-membrane vesicles.Systematic assembly of a full-length infectious cDNA of mouse hepatitis virus strain A59.Bovine coronavirus 5'-proximal genomic acceptor hotspot for discontinuous transcription is 65 nucleotides wide.Dodecamer structure of severe acute respiratory syndrome coronavirus nonstructural protein nsp10.Construction of a severe acute respiratory syndrome coronavirus infectious cDNA clone and a replicon to study coronavirus RNA synthesis.SARS--beginning to understand a new virus.Human coronavirus 229E papain-like proteases have overlapping specificities but distinct functions in viral replication.Antiviral applications of RNAi for coronavirus.Genome organization and reverse genetic analysis of a type I feline coronavirusComparative in vivo analysis of the nsp15 endoribonuclease of murine, porcine and severe acute respiratory syndrome coronaviruses.Characterization of a critical interaction between the coronavirus nucleocapsid protein and nonstructural protein 3 of the viral replicase-transcriptase complex.Major genetic marker of nidoviruses encodes a replicative endoribonucleasePorcine Epidemic Diarrhea Virus 3C-Like Protease-Mediated Nucleocapsid Processing: Possible Link to Viral Cell Culture Adaptability.Structural and biochemical basis for the difference in the helicase activity of two different constructs of SARS-CoV helicase.A new cistron in the murine hepatitis virus replicase gene.Functional and genetic studies of the substrate specificity of coronavirus infectious bronchitis virus 3C-like proteinase.Multigene RNA vector based on coronavirus transcription.The nucleoprotein is required for efficient coronavirus genome replication.A complex zinc finger controls the enzymatic activities of nidovirus helicasesMass spectroscopic characterization of the coronavirus infectious bronchitis virus nucleoprotein and elucidation of the role of phosphorylation in RNA binding by using surface plasmon resonance.The autocatalytic release of a putative RNA virus transcription factor from its polyprotein precursor involves two paralogous papain-like proteases that cleave the same peptide bond.Multiple enzymatic activities associated with severe acute respiratory syndrome coronavirus helicase.Membrane topology of murine coronavirus replicase nonstructural protein 3.Coronavirus nonstructural protein 16 is a cap-0 binding enzyme possessing (nucleoside-2'O)-methyltransferase activity.
P2860
Q21558776-3938A66F-1A2B-431A-B2E3-9275E93F3048Q24530697-11FAA2D5-C5E3-45DB-9E6D-19716A8484BAQ26863163-4D384DD1-9C35-4D92-8FAB-408A3083F73BQ27477549-067D83B3-A713-41CE-B46E-BF3721CEA3F5Q27641043-E1A1E329-38BF-485F-B7F0-6E0D200DB949Q27642450-DF0FF029-2914-4875-9864-F79EBA221E8BQ27653024-496D59C7-B61D-48C6-8A5A-0E4C15179122Q27675449-99FA2C0F-6525-4456-B6F2-BDB38E359F3AQ27701581-E79D71F4-B75D-4418-9647-155AFC800E0AQ30352512-614FD225-3BFE-415E-8BF6-9D9D5E58608BQ33614644-6F0C2DF7-3EE3-4DCD-96BD-8CF95D469D8DQ33788868-30684CA6-C6C5-400C-A670-9C2A86645EF3Q33826694-717C87E6-F995-4328-B720-80C10DDFAF1BQ34102257-3AA96066-EC75-4A96-83D8-CB0C7E807F19Q34120658-285C755D-8090-4FE4-ABD5-DDFAAE1E9B16Q34332580-1E53BCAF-56C3-4B68-B38A-534825302E2CQ34336367-3237D13C-E2F5-41B6-92A1-E4638C97BBA4Q34348993-752A8D4B-CB0A-4BD6-AE19-0FEDC18DFD20Q34434740-30BE0055-C621-4F74-B917-4105DD2764DFQ35024043-CAD548B2-70CB-4674-88E0-95C2492A7A39Q35139215-5B48C9EB-C215-4848-A013-16BDBD5AED59Q35701656-600239A6-CE83-4F3E-BFE0-6B65D4C83395Q35785423-1BDD7B5E-4810-42A0-BF9C-22D50BCAF962Q36376425-BEC8C27C-AD25-49B2-9F9E-1C3752E48C86Q36483272-4F2BD672-240C-4F0A-9AEA-6D69D9A38619Q36517228-AEC414F1-F533-4458-9EFD-F58E99D77275Q37123379-E27718A4-ACA3-4121-A29E-B238D7309744Q37487223-F8910537-7987-490C-8575-6F09C70C4FBEQ37560777-686D3F9F-8D00-477A-8C34-C789C30D18C7Q39444016-8BD267F7-7498-42B7-8D96-51D9C2626E97Q39674266-0B3A8439-F2C3-475A-882D-A6C37A2B71CFQ39707305-F754C267-8E70-4485-B050-8297ABB175C4Q39996428-63F5E8E2-88DC-43A5-8AD4-B528FF7BCFA1Q40276750-933132F4-9F39-490C-8333-FDE73DEEF4F8Q40722819-E3EF3A49-1AF2-4E46-8F51-2A3A6F793CC9Q40723706-61061346-5E85-4C37-8AD5-9A8376BEE944Q40795681-2BE8BAEF-C85E-4A2A-93AC-1E431FC65E03Q40883770-D44EDEB8-827E-40C9-9F2F-CA2C84396C84Q41885804-C842AFFF-6B6E-4F61-9DE7-533454C02634Q42406865-04169DC0-F79F-45CF-9651-BD91B1648FC6
P2860
Viral replicase gene products suffice for coronavirus discontinuous transcription.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Viral replicase gene products suffice for coronavirus discontinuous transcription.
@en
Viral replicase gene products suffice for coronavirus discontinuous transcription.
@nl
type
label
Viral replicase gene products suffice for coronavirus discontinuous transcription.
@en
Viral replicase gene products suffice for coronavirus discontinuous transcription.
@nl
prefLabel
Viral replicase gene products suffice for coronavirus discontinuous transcription.
@en
Viral replicase gene products suffice for coronavirus discontinuous transcription.
@nl
P2093
P2860
P1433
P1476
Viral replicase gene products suffice for coronavirus discontinuous transcription.
@en
P2093
P2860
P304
P356
10.1128/JVI.75.14.6676-6681.2001
P407
P577
2001-07-01T00:00:00Z