Genome polyprotein
Details
- Name
- Genome polyprotein
- Synonyms
- 3.4.22.29
- P2A
- Gene Name
- Not Available
- Organism
- HRV-16
- Amino acid sequence
>lcl|BSEQ0012798|Genome polyprotein MGAQVSRQNVGTHSTQNMVSNGSSLNYFNINYFKDAASSGASRLDFSQDPSKFTDPVKDV LEKGIPTLQSPSVEACGYSDRIIQITRGDSTITSQDVANAVVGYGVWPHYLTPQDATAID KPTQPDTSSNRFYTLDSKMWNSTSKGWWWKLPDALKDMGIFGENMFYHFLGRSGYTVHVQ CNASKFHQGTLLVVMIPEHQLATVNKGNVNAGYKYTHPGEAGREVGTQVENEKQPSDDNW LNFDGTLLGNLLIFPHQFINLRSNNSATLIVPYVNAVPMDSMVRHNNWSLVIIPVCQLQS NNISNIVPITVSISPMCAEFSGARAKTVVQGLPVYVTPGSGQFMTTDDMQSPCALPWYHP TKEIFIPGEVKNLIEMCQVDTLIPINSTQSNIGNVSMYTVTLSPQTKLAEEIFAIKVDIA SHPLATTLIGEIASYFTHWTGSLRFSFMFCGTANTTLKVLLAYTPPGIGKPRSRKEAMLG THVVWDVGLQSTVSLVVPWISASQYRFTTPDTYSSAGYITCWYQTNFVVPPNTPNTAEML CFVSGCKDFCLRMARDTDLHKQTGPITQNPVERYVDEVLNEVLVVPNINQSHPTTSNAAP VLDAAETGHTNKIQPEDTIETRYVQSSQTLDEMSVESFLGRSGCIHESVLDIVDNYNDQS FTKWNINLQEMAQIRRKFEMFTYARFDSEITMVPSVAAKDGHIGHIVMQYMYVPPGAPIP TTRDDYAWQSGTNASVFWQHGQPFPRFSLPFLSIASAYYMFYDGYDGDTYKSRYGTVVTN DMGTLCSRIVTSEQLHKVKVVTRIYHKAKHTKAWCPRPPRAVQYSHTHTTNYKLSSEVHN DVAIRPRTNLTTVGPSDMYVHVGNLIYRNLHLFNSDIHDSILVSYSSDLIIYRTSTQGDG YIPTCNCTEATYYCKHKNRYYPINVTPHDWYEIQESEYYPKHIQYNLLIGEGPCEPGDCG GKLLCKHGVIGIITAGGEGHVAFIDLRHFHCAEEQGITDYIHMLGEAFGSGFVDSVKDQI NSINPINNISSKMVKWMLRIISAMVIIIRNSSDPQTIIATLTLIGCNGSPWRFLKEKFCK WTQLTYIHKESDSWLKKFTEMCNAARGLEWIGNKISKFIDWMKSMLPQAQLKVKYLSELK KLNFLEKQVENLRAADTNTQEKIKCEIDTLHDLSCKFLPLYASEAKRIKVLYHKCTNIIK QKKRSEPVAVMIHGPPGTGKSITTSFLARMITNESDIYSLPPDPKYFDGYDNQSVVIMDD IMQNPGGEDMTLFCQMVSSVTFIPPMADLPDKGKPFDSRFVLCSTNHSLLAPPTISSLPA MNRRFYLDLDILVHDNYKDNQGKLDVSRAFRLCDVDSKIGNAKCCPFVCGKAVTFKDRNT CRTYSLSQIYNQILEEDKRRRQVVDVMSAIFQGPISMDKPPPPAITDLLRSVRTPEVIKY CQDNKWIVPADCQIERDLNIANSIITIIANIISIAGIIYIIYKLFCSLQGPYSGEPKPKT KVPERRVVAQGPEEEFGMSIIKNNTCVVTTTNGKFTGLGIYDRILILPTHADPGSEIQVN GIHTKVLDSYDLFNKEGVKLEITVLKLDRNEKFRDIRKYIPESEDDYPECNLALVANQTE PTIIKVGDVVSYGNILLSGTQTARMLKYNYPTKSGYCGGVLYKIGQILGIHVGGNGRDGF SSMLLRSYFTEQQGQIQISKHVKDVGLPSIHTPTKTKLQPSVFYDIFPGSKEPAVLTEKD PRLKVDFDSALFSKYKGNTECSLNEHIQVAVAHYSAQLATLDIDPQPIAMEDSVFGMDGL EALDLNTSAGYPYVTLGIKKKDLINNKTKDISKLKLALDKYDVDLPMITFLKDELRKKDK IAAGKTRVIEASSINDTILFRTVYGNLFSKFHLNPGVVTGCAVGCDPETFWSKIPLMLDG DCIMAFDYTNYDGSIHPIWFKALGMVLDNLSFNPTLINRLCNSKHIFKSTYYEVEGGVPS GCSGTSIFNSMINNIIIRTLVLDAYKHIDLDKLKIIAYGDDVIFSYKYKLDMEAIAKEGQ KYGLTITPADKSSEFKELDYGNVTFLKRGFRQDDKYKFLIHPTFPVEEIYESIRWTKKPS QMQEHVLSLCHLMWHNGPEIYKDFETKIRSVSAGRALYIPPYELLRHEWYEKF
- Number of residues
- 2153
- Molecular Weight
- 242242.05
- Theoretical pI
- 7.1
- GO Classification
- FunctionsATP binding / cysteine-type endopeptidase activity / ion channel activity / RNA binding / RNA helicase activity / RNA-directed RNA polymerase activity / structural molecule activityProcessesDNA replication / endocytosis involved in viral entry into host cell / induction by virus of host autophagy / pore formation by virus in membrane of host cell / pore-mediated entry of viral genome into host cell / positive stranded viral RNA replication / protein oligomerization / RNA-protein covalent cross-linking / suppression by virus of host gene expression / suppression by virus of host mRNA export from nucleus / suppression by virus of host RIG-I activity by RIG-I proteolysis / suppression by virus of host translation initiation factor activity / transcription, DNA-templated / viral RNA genome replication / virion attachment to host cellComponentshost cell cytoplasmic vesicle membrane / integral to membrane of host cell / membrane / T=pseudo3 icosahedral viral capsid
- General Function
- Structural molecule activity
- Specific Function
- Capsid protein VP1: Forms an icosahedral capsid of pseudo T=3 symmetry with capsid proteins VP2 and VP3. The capsid is 300 Angstroms in diameter, composed of 60 copies of each capsid protein and enclosing the viral positive strand RNA genome. Capsid protein VP1 mainly forms the vertices of the capsid. Capsid protein VP1 interacts with host cell receptor to provide virion attachment to target host cells. This attachment induces virion internalization. Tyrosine kinases are probably involved in the entry process. After binding to its receptor, the capsid undergoes conformational changes. Capsid protein VP1 N-terminus (that contains an amphipathic alpha-helix) and capsid protein VP4 are externalized. Together, they shape a pore in the host membrane through which viral genome is translocated to host cell cytoplasm. After genome has been released, the channel shrinks (By similarity).Capsid protein VP2: Forms an icosahedral capsid of pseudo T=3 symmetry with capsid proteins VP2 and VP3. The capsid is 300 Angstroms in diameter, composed of 60 copies of each capsid protein and enclosing the viral positive strand RNA genome (By similarity).Capsid protein VP3: Forms an icosahedral capsid of pseudo T=3 symmetry with capsid proteins VP2 and VP3. The capsid is 300 Angstroms in diameter, composed of 60 copies of each capsid protein and enclosing the viral positive strand RNA genome (By similarity).Capsid protein VP4: Lies on the inner surface of the capsid shell. After binding to the host receptor, the capsid undergoes conformational changes. Capsid protein VP4 is released, Capsid protein VP1 N-terminus is externalized, and together, they shape a pore in the host membrane through which the viral genome is translocated into the host cell cytoplasm. After genome has been released, the channel shrinks (By similarity).Capsid protein VP0: Component of immature procapsids, which is cleaved into capsid proteins VP4 and VP2 after maturation. Allows the capsid to remain inactive before the maturation step (By similarity).Protein 2A: Cysteine protease that cleaves viral polyprotein and specific host proteins. It is responsible for the cleavage between the P1 and P2 regions, first cleavage occurring in the polyprotein. Cleaves also the host translation initiation factor EIF4G1, in order to shut down the capped cellular mRNA translation. Inhibits the host nucleus-cytoplasm protein and RNA trafficking by cleaving host members of the nuclear pores (By similarity).Protein 2B: Plays an essential role in the virus replication cycle by acting as a viroporin. Creates a pore in the host reticulum endoplasmic and as a consequence releases Ca2+ in the cytoplasm of infected cell. In turn, high levels of cyctoplasmic calcium may trigger membrane trafficking and transport of viral ER-associated proteins to viroplasms, sites of viral genome replication (By similarity).Protein 2C: Induces and associates with structural rearrangements of intracellular membranes. Displays RNA-binding, nucleotide binding and NTPase activities. May play a role in virion morphogenesis and viral RNA encapsidation by interacting with the capsid protein VP3 (By similarity).Protein 3AB: Localizes the viral replication complex to the surface of membranous vesicles. Together with protein 3CD binds the Cis-Active RNA Element (CRE) which is involved in RNA synthesis initiation. Acts as a cofactor to stimulate the activity of 3D polymerase, maybe through a nucleid acid chaperone activity (By similarity).Protein 3A: Localizes the viral replication complex to the surface of membranous vesicles. It inhibits host cell endoplasmic reticulum-to-Golgi apparatus transport and causes the dissassembly of the Golgi complex, possibly through GBF1 interaction. This would result in depletion of MHC, trail receptors and IFN receptors at the host cell surface (By similarity).Viral protein genome-linked: acts as a primer for viral RNA replication and remains covalently bound to viral genomic RNA. VPg is uridylylated prior to priming replication into VPg-pUpU. The oriI viral genomic sequence may act as a template for this. The VPg-pUpU is then used as primer on the genomic RNA poly(A) by the RNA-dependent RNA polymerase to replicate the viral genome. VPg may be removed in the cytoplasm by an unknown enzyme termed "unlinkase". VPg is not cleaved off virion genomes because replicated genomic RNA are encapsidated at the site of replication (By similarity).Protein 3CD: Is involved in the viral replication complex and viral polypeptide maturation. It exhibits protease activity with a specificity and catalytic efficiency that is different from protease 3C. Protein 3CD lacks polymerase activity. The 3C domain in the context of protein 3CD may have an RNA binding activity (By similarity).Protease 3C: cleaves host DDX58/RIG-I and thus contributes to the inhibition of type I interferon production. Cleaves also host PABPC1 (By similarity).RNA-directed RNA polymerase: Replicates the viral genomic RNA on the surface of intracellular membranes. May form linear arrays of subunits that propagate along a strong head-to-tail interaction called interface-I. Covalently attaches UMP to a tyrosine of VPg, which is used to prime RNA synthesis. The positive stranded RNA genome is first replicated at virus induced membranous vesicles, creating a dsRNA genomic replication form. This dsRNA is then used as template to synthesize positive stranded RNA genomes. ss(+)RNA genomes are either translated, replicated or encapsidated (By similarity).
- Pfam Domain Function
- Transmembrane Regions
- Not Available
- Cellular Location
- Virion
- Gene sequence
>lcl|BSEQ0007678|6462 bp ATGGGCGCTCAAGTATCTAGACAGAATGTTGGTACGCACTCAACACAAAATATGGTGTCA AATGGATCCAGCCTCAATTATTTTAACATTAATTATTTCAAAGATGCAGCTTCCAGTGGT GCTTCTCGATTGGACTTCTCTCAAGACCCCAGTAAATTCACAGACCCAGTTAAGGATGTG TTGGAGAAAGGCATACCCACTCTGCAATCTCCAAGTGTAGAAGCTTGTGGATACTCTGAT AGAATAATCCAAATTACAAGAGGCGACTCAACCATAACATCTCAAGATGTTGCTAATGCA GTGGTTGGGTATGGGGTATGGCCACACTACCTAACTCCGCAGGATGCAACGGCTATAGAC AAGCCAACACAACCAGATACATCATCAAATAGGTTTTACACACTGGATAGTAAAATGTGG AACAGTACCTCCAAAGGTTGGTGGTGGAAACTACCAGATGCTCTTAAAGACATGGGTATT TTTGGTGAAAATATGTTTTATCATTTCTTGGGTAGAAGTGGTTATACAGTGCACGTACAG TGCAATGCAAGTAAATTCCACCAGGGTACACTACTAGTGGTTATGATACCAGAACACCAG TTAGCTACAGTAAATAAAGGTAATGTTAATGCAGGTTACAAATACACACATCCTGGTGAA GCTGGTAGAGAAGTGGGTACACAAGTTGAAAATGAGAAACAACCTAGTGATGATAATTGG CTAAATTTTGATGGTACATTATTGGGCAATTTACTGATATTCCCACACCAGTTTATTAAC TTAAGGAGCAATAACTCAGCAACTCTTATAGTACCATATGTTAATGCTGTTCCAATGGAT TCTATGGTTAGACATAACAATTGGAGTTTGGTAATAATACCAGTTTGTCAACTACAAAGC AACAATATATCCAACATTGTTCCCATCACTGTTTCCATTAGCCCAATGTGTGCTGAATTC TCTGGAGCACGTGCCAAAACAGTTGTGCAAGGTCTACCAGTATATGTTACACCAGGATCA GGACAATTCATGACAACAGATGATATGCAATCTCCATGTGCACTGCCTTGGTACCATCCA ACAAAAGAGATCTTTATACCAGGAGAGGTTAAGAACTTGATTGAAATGTGTCAGGTGGAT ACACTCATACCAATAAATAGCACACAGTCTAACATTGGCAATGTCAGCATGTACACAGTA ACTCTATCACCACAAACAAAATTAGCTGAAGAAATTTTTGCAATTAAAGTAGATATTGCC TCACATCCCTTAGCCACAACCCTCATTGGTGAGATAGCAAGTTACTTTACACACTGGACA GGGAGCCTGCGATTCAGTTTCATGTTTTGCGGGACTGCAAACACTACCTTAAAAGTTTTG CTAGCATATACACCCCCAGGGATTGGTAAGCCTAGAAGTAGAAAGGAAGCAATGTTAGGG ACACACGTGGTGTGGGATGTAGGTTTACAATCTACAGTGTCATTGGTTGTACCATGGATC AGTGCCAGTCAGTATAGATTCACTACACCAGACACATACTCCTCAGCAGGCTACATTACA TGCTGGTATCAAACTAATTTTGTTGTTCCACCAAACACACCTAACACTGCTGAGATGTTG TGTTTTGTATCTGGATGCAACCACTTTTGCCTTCGGATGGCAAGAGACACAGACCTGCAC AAGCAAACAGGACCAATAACACAAAATCCAGTGGAAAGATATGTAGATGAAGTCTTAAAT GAAGTGTTAGTAGTGCCCAATATTAATCAGAGCCACCCTACCACATCAAATGCAGCCCCA GTTTTGGATGCTGCTGAAACAGGACATACCAATAAGATACAGCCAGAAGACACTATAGAA ACCAGATATGTGCAATCTTCACAGACATTGGATGAAATGAGTGTGGAAAGCTTCCTAGGC AGATCGGGGTGCATCCATGAATCAGTGTTGGATATTGTGGACAATTACAATGATCAAAGT TTCACTAAATGGAACATAAACCTGCAAGAAATGGCACAAATTAGAAGAAAATTTGAAATG TTTACTTATGCAAGATTTGACTCTGAAATTACTATGGTACCAAGTGTAGCAGCCAAAGAT GGTCACATTGGTCATATAGTCATGCAATATATGTATGTACCACCAGGAGCACCTATACCA ACAACTAGAGATGACTATGCTTGGCAATCTGGAACAAATGCATCTGTATTTTGGCAGCAT GGGCAACCTTTCCCTCGCTTTTCACTTCCCTTTTTGAGTATTGCATCAGCATATTACATG TTTTATGATGGTTATGATGGAGACACATATAAATCCAGATATGGAACTGTAGTCACCAAT GACATGGGAACTTTGTGTTCGCGTATTGTGACCAGTGAGCAATTACACAAAGTCAAAGTG GTAACAAGGATATATCACAAAGCCAAACACACCAAAGCTTGGTGCCCAAGACCACCCAGA GCTGTTCAATACTCACATACACATACCACCAACTACAAATTGAGTTCAGAAGTACACAAT GATGTGGCTATAAGACCTAGAACAAATCTAACAACTGTTGGGCCTAGTGACATGTATGTG CATGTTGGTAATCTAATATACAGAAATCTACATTTATTTAACTCTGACATACATGATTCC ATTTTAGTGTCTTATTCATCAGATTTAATCATATACCGAACAAGCACACAAGGTGATGGT TATATTCCAACATGTAATTGCACTGAAGCTACATATTACTGCAAACACAAAAACAGGTAC TACCCAATTAATGTCACACCTCATGACTGGTATGAGATACAAGAGAGTGAATATTATCCA AAACATATCCAGTACAATTTACTAATAGGTGAAGGACCATGTGAACCAGGTGATTGTGGT GGGAAATTATTATGCAAACATGGAGTGATAGGTATTATTACAGCAGGTGGTGAGGGCCAT GTTGCATTCATAGATCTTAGACACTTTCACTGTGCTGAAGAACAAGGAATCACTGATTAC ATACACATGCTCGGTGAAGCTTTTGGTAGTGGATTTGTAGATAGTGTTAAAGACCAGATT AATTCAATAAATCCCATCAATAACATTAGCAGTAAGATGGTTAAATGGATGTTAAGAATT ATATCAGCTATGGTTATAATTATTAGAAACTCTTCAGATCCGCAAACAATAATTGCCACT TTAACACTGATTGGATGCAATGGTTCTCCTTGGAGATTTCTCAAAGAAAAGTTCTGTAAA TGGACTCAATTAACTTATATACACAAAGAATCAGATTCATGGCTCAAAAAATTCACTGAG ATGTGTAATGCAGCTAGGGGGCTAGAATGGATTGGAAACAAAATATCCAAATTTATCGAT TGGATGAAATCAATGCTACCCCAGGCACAATTAAAAGTTAAGTATTTGAGTGAACTTAAG AAACTCAACTTTCTGGAGAAACAGGTTGAAAATCTCAGAGCAGCTGATACTAACACTCAA GAAAAAATCAAGTGTGAGATAGATACATTGCATGACTTATCCTGTAAGTTTTTACCTCTG TATGCCAGTGAAGCAAAGAGAATTAAAGTGTTGTATCACAAGTGCACTAACATAATTAAA CAGAAGAAGAGAAGTGAACCTGTAGCAGTTATGATACACGGGCCTCCTGGGACCGGAAAA TCAATCACTACAAGCTTCCTGGCTAGAATGATTACTAATGAGAGTGACATATACTCACTT CCACCAGACCCTAAATATTTTGATGGTTATGATAACCAGAGTGTAGTAATAATGGATGAC ATCATGCAAAACCCTGGTGGTGAGGACATGACATTATTCTGTCAGATGGTATCTAGTGTG ACTTTTATACCCCCAATGGCTGATCTACCAGATAAGGGAAAACCCTTTGATTCTAGATTT GTATTGTGTAGTACTAATCACTCACTCTTGGCACCCCCAACTATATCGTCGCTCCCAGCA ATGAATAGAAGATTCTATTTAGATTTAGATATTCTTGTGCATGATAACTACAAAGATAAT CAGGGTAAGTTAGATGTTTCTAGAGCATTTCGGCTATGTGATGTTGATTCAAAGATTGGA AATGCAAAATGTTGTCCATTTGTATGTGGCAAGGCAGTGACATTCAAGGACCGCAACACA TGTAGAACTTATTCACTTTCCCAAATATACAACCAAATTCTTGAGGAAGACAAGAGAAGG AGACAGGTGGTTGATGTCATGTCTGCAATTTTCCAAGGGCCTATATCCATGGATAAACCC CCACCACCAGCTATAACAGACCTTTTACGCTCAGTAAGGACACCAGAAGTAATTAAGTAC TGCCAAGACAATAAATGGATAGTTCCTGCGGACTGCCAAATTGAAAGGGATCTGAATATA GCTAATAGCATAATCACAATCATAGCTAATATCATCAGTATAGCAGGGATTATATATATA ATTTATAAGCTCTTTTGCTCTCTACAGGGCCCTTACTCGGGGGAGCCCAAACCTAAGACA AAAGTTCCCGAGAGAAGAGTGGTAGCTCAAGGTCCAGAAGAAGAATTTGGAATGTCTATT ATTAAAAATAATACCTGTGTTGTGACCACAACAAATGGAAAATTTACAGGATTAGGCATT TATGACAGAATCTTAATATTACCAACACATGCTGACCCGGGCAGTGAAATTCAAGTAAAT GGAATACACACCAAAGTGCTTGATTCTTATGACTTATTTAATAAGGAAGGTGTCAAGTTG GAAATTACTGTGCTAAAGTTAGATAGAAATGAGAAGTTCAGGGATATACGTAAGTACATA CCTGAATCAGAAGATGACTATCCTGAATGCAACCTAGCACTAGTGGCCAATCAAACAGAA CCAACTATAATCAAAGTAGGGGATGTTGTGTCTTATGGTAATATATTACTTAGTGGCACA CAGACAGCCAGAATGCTTAAATATAACTATCCTACAAAATCTGGGTATTGTGGTGGTGTG TTATACAAGATTGGCCAGATCTTAGGTATACATGTGGGTGGCAATGGTAGAGATGGGTTT TCATCTATGCTATTGAGATCATACTTCACTGAACAACAAGGCCAAATTCAAATCTCTAAA CATGTTAAAGATGTTGGCTTACCCTCAATACATACGCCAACTAAAACTAAATTGCAGCCA AGTGTCTTCTATGACATTTTTCCAGGCAGTAAGGAACCAGCAGTCCTCACAGAAAAAGAT CCTAGATTGAAAGTGGACTTTGACTCAGCTCTTTTTTCAAAATACAAAGGTAACACAGAG TGCAGTTTGAATGAACATATACAAGTTGCAGTAGCACACTACTCAGCTCAGCTAGCAACA CTAGATATAGATCCACAACCAATTGCAATGGAAGATAGTGTTTTTGGAATGGATGGCTTG GAAGCTTTGGATCTGAATACTAGTGCAGGTTATCCCTATGTAACACTAGGAATTAAAAAG AAAGATCTTATTAATAACAAGACTAAAGATATTTCCAAACTTAAGCTAGCATTAGACAAA TATGATGTTGATTTGCCCATGATTACTTTCTTAAAAGATGAACTTAGAAAGAAGGATAAG ATAGCAGCAGGCAAAACCAGAGTTATAGAAGCTAGTAGTATAAATGATACCATTTTGTTT AGAACAGTTTATGGAAACCTATTTTCTAAATTTCACTTGAACCCAGGAGTGGTAACAGGC TGTGCAGTTGGATGTGATCCAGAAACCTTTTGGTCTAAAATTCCCTTGATGTTAGATGGA GATTGCATCATGGCTTTTGATTATACAAATTATGATGGTAGCATTCATCCAATTTGGTTT AAAGCTCTCGGGATGGTACTTGATAATTTATCCTTTAACCCTACTCTAATCAATAGACTT TGTAACTCAAAACATATTTTCAAGTCCACATATTATGAAGTTGAAGGTGGTGTGCCCTCT GGTTGTTCTGGAACTAGTATATTTAACTCAATGATTAATAATATAATCATTAGAACCTTA GTTTTGGATGCATATAAACATATTGATTTAGATAAACTTAAAATAATTGCCTATGGTGAT GATGTGATCTTTTCTTACAAGTATAAACTAGACATGGAAGCCATAGCCAAGGAAGGGCAG AAATATGGACTTACTATAACACCTGCAGATAAATCTAGTGAATTCAAAGAACTTGATTAT GGAAATGTAACTTTTCTTAAAAGAGGATTTAGACAAGATGATAAATACAAATTTTTGATA CATCCTACTTTTCCAGTTGAAGAGATTTATGAGTCCATTAGATGGACAAAGAAACCATCT CAAATGCAGGAGCATGTCTTATCCTTGTGTCACTTAATGTGGCACAATGGTCCTGAGATT TATAAGGACTTTGAAACAAAGATACGCAGTGTCAGCGCTGGACGTGCACTGTATATCCCT CCTTATGAACTCCTAAGACATGAATGGTATGAAAAATTCTAG
- Chromosome Location
- Not Available
- Locus
- Not Available
- External Identifiers
Resource Link UniProtKB ID Q82122 UniProtKB Entry Name POLG_HRV16 GenBank Protein ID 409464 GenBank Gene ID L24917 - General References
- Lee WM, Wang W, Rueckert RR: Complete sequence of the RNA genome of human rhinovirus 16, a clinically useful common cold virus belonging to the ICAM-1 receptor group. Virus Genes. 1995 Jan;9(2):177-81. [Article]
- Ghildyal R, Jordan B, Li D, Dagher H, Bardin PG, Gern JE, Jans DA: Rhinovirus 3C protease can localize in the nucleus and alter active and passive nucleocytoplasmic transport. J Virol. 2009 Jul;83(14):7349-52. doi: 10.1128/JVI.01748-08. Epub 2009 Apr 29. [Article]
- Fuchs R, Blaas D: Productive entry pathways of human rhinoviruses. Adv Virol. 2012;2012:826301. doi: 10.1155/2012/826301. Epub 2012 Nov 26. [Article]
- Oliveira MA, Zhao R, Lee WM, Kremer MJ, Minor I, Rueckert RR, Diana GD, Pevear DC, Dutko FJ, McKinlay MA, et al.: The structure of human rhinovirus 16. Structure. 1993 Sep 15;1(1):51-68. [Article]
- Hadfield AT, Lee Wm, Zhao R, Oliveira MA, Minor I, Rueckert RR, Rossmann MG: The refined structure of human rhinovirus 16 at 2.15 A resolution: implications for the viral life cycle. Structure. 1997 Mar 15;5(3):427-41. [Article]
Drug Relations
- Drug Relations
DrugBank ID Name Drug group Pharmacological action? Actions Details DB03017 Lauric acid approved, experimental unknown Details DB08231 Myristic acid experimental unknown Details DB08713 2,6-DIMETHYL-1-(3-[3-METHYL-5-ISOXAZOLYL]-PROPANYL)-4-[2N-METHYL-2H-TETRAZOL-5-YL]-PHENOL experimental unknown Details DB08714 2,6-DIMETHYL-1-(3-[3-METHYL-5-ISOXAZOLYL]-PROPANYL)-4-[4-METHYL-2H-TETRAZOL-2-YL]-PHENOL experimental unknown Details DB08715 2,6-DIMETHYL-1-(3-[3-METHYL-5-ISOXAZOLYL]-PROPANYL)-4-[2-METHYL-4-ISOXAZOLYL]-PHENOL experimental unknown Details