Physical interaction between the herpes simplex virus type 1 immediate-early regulatory proteins ICP0 and ICP4.
about
ICP0 dismantles microtubule networks in herpes simplex virus-infected cellsICP0 antagonizes ICP4-dependent silencing of the herpes simplex virus ICP0 geneA novel cellular protein, p60, interacting with both herpes simplex virus 1 regulatory proteins ICP22 and ICP0 is modified in a cell-type-specific manner and Is recruited to the nucleus after infectionDetermination of interactions between tegument proteins of herpes simplex virus type 1Herpes simplex virus type 1 immediate-early protein ICP27 is required for efficient incorporation of ICP0 and ICP4 into virionsInteraction of the equine herpesvirus 1 EICP0 protein with the immediate-early (IE) protein, TFIIB, and TBP may mediate the antagonism between the IE and EICP0 proteinsPosttranslational processing of infected cell proteins 0 and 4 of herpes simplex virus 1 is sequential and reflects the subcellular compartment in which the proteins localizeDefinition of herpes simplex virus type 1 helper activities for adeno-associated virus early replication eventsICP0 induces the accumulation of colocalizing conjugated ubiquitin.Characterization of the trans-activation properties of equine herpesvirus 1 EICP0 proteinDeletion of the herpes simplex virus VP22-encoding gene (UL49) alters the expression, localization, and virion incorporation of ICP0.The dominant-negative herpes simplex virus type 1 (HSV-1) recombinant CJ83193 can serve as an effective vaccine against wild-type HSV-1 infection in mice.Composition of pseudorabies virus particles lacking tegument protein US3, UL47, or UL49 or envelope glycoprotein E.Identification of TRIM27 as a novel degradation target of herpes simplex virus 1 ICP0.Herpes simplex virus immediate-early protein ICP0 is targeted by SIAH-1 for proteasomal degradation.Role of ICP0 in the strategy of conquest of the host cell by herpes simplex virus 1The C-terminal repressor region of herpes simplex virus type 1 ICP27 is required for the redistribution of small nuclear ribonucleoprotein particles and splicing factor SC35; however, these alterations are not sufficient to inhibit host cell splicinAn activity specified by the osteosarcoma line U2OS can substitute functionally for ICP0, a major regulatory protein of herpes simplex virus type 1Herpes simplex virus trans-regulatory protein ICP27 stabilizes and binds to 3' ends of labile mRNA.Attenuation of DNA-dependent protein kinase activity and its catalytic subunit by the herpes simplex virus type 1 transactivator ICP0.The ICP0 protein of equine herpesvirus 1 is an early protein that independently transactivates expression of all classes of viral promoters.Translocation and colocalization of ICP4 and ICP0 in cells infected with herpes simplex virus 1 mutants lacking glycoprotein E, glycoprotein I, or the virion host shutoff product of the UL41 gene.Binding partners for the UL11 tegument protein of herpes simplex virus type 1.High-level expression of glycoprotein D by a dominant-negative HSV-1 virus augments its efficacy as a vaccine against HSV-1 infection.A negative regulatory element (base pairs -204 to -177) of the EICP0 promoter of equine herpesvirus 1 abolishes the EICP0 protein's trans-activation of its own promoter.Cellular unfolded protein response against viruses used in gene therapyThe NH2 terminus of the herpes simplex virus type 1 regulatory protein ICP0 contains a promoter-specific transcription activation domain.Cellular Protein WDR11 Interacts with Specific Herpes Simplex Virus Proteins at the trans-Golgi Network To Promote Virus Replication.Herpes simplex virus 1 ICP4 forms complexes with TFIID and mediator in virus-infected cellsIdentification of a motif in the C terminus of herpes simplex virus regulatory protein ICP4 that contributes to activation of transcriptionHerpes simplex virus type 1 immediate-early protein ICP0 and is isolated RING finger domain act as ubiquitin E3 ligases in vitro.Mutational analysis of ICP0R, a transrepressor protein created by alternative splicing of the ICP0 gene of herpes simplex virus type 1.Physical and functional interactions between herpes simplex virus immediate-early proteins ICP4 and ICP27.Activation of gene expression by herpes simplex virus type 1 ICP0 occurs at the level of mRNA synthesis.The UL14 tegument protein of herpes simplex virus type 1 is required for efficient nuclear transport of the alpha transinducing factor VP16 and viral capsids.DNA-dependent oligomerization of herpes simplex virus type 1 regulatory protein ICP4Herpes simplex virus-1 disarms the unfolded protein response in the early stages of infection.
P2860
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P2860
Physical interaction between the herpes simplex virus type 1 immediate-early regulatory proteins ICP0 and ICP4.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Physical interaction between t ...... latory proteins ICP0 and ICP4.
@ast
Physical interaction between t ...... latory proteins ICP0 and ICP4.
@en
type
label
Physical interaction between t ...... latory proteins ICP0 and ICP4.
@ast
Physical interaction between t ...... latory proteins ICP0 and ICP4.
@en
prefLabel
Physical interaction between t ...... latory proteins ICP0 and ICP4.
@ast
Physical interaction between t ...... latory proteins ICP0 and ICP4.
@en
P2860
P1433
P1476
Physical interaction between t ...... latory proteins ICP0 and ICP4.
@en
P2093
P2860
P304
P407
P577
1994-12-01T00:00:00Z