Specific destruction of kinetochore protein CENP-C and disruption of cell division by herpes simplex virus immediate-early protein Vmw110.
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ICP0 dismantles microtubule networks in herpes simplex virus-infected cellsICP0 antagonizes ICP4-dependent silencing of the herpes simplex virus ICP0 geneRING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitinationThe bovine herpesvirus 1 immediate-early protein (bICP0) associates with histone deacetylase 1 to activate transcription.The infected cell protein 0 encoded by bovine herpesvirus 1 (bICP0) associates with interferon regulatory factor 7 and consequently inhibits beta interferon promoter activitySubcellular recruitment of fibrillarin to nucleoplasmic proteasomes: implications for processing of a nucleolar autoantigen.Ariadne-1: a vital Drosophila gene is required in development and defines a new conserved family of ring-finger proteinsThe herpes simplex virus ICP0 RING finger domain inhibits IRF3- and IRF7-mediated activation of interferon-stimulated genesDeath receptor-induced apoptosis reveals a novel interplay between the chromosomal passenger complex and CENP-C during interphaseThe degradation of promyelocytic leukemia and Sp100 proteins by herpes simplex virus 1 is mediated by the ubiquitin-conjugating enzyme UbcH5aInfected cell protein 0 functional domains and their coordination in herpes simplex virus replicationThe potential link between PML NBs and ICP0 in regulating lytic and latent infection of HSV-1A viral E3 ligase targets RNF8 and RNF168 to control histone ubiquitination and DNA damage responsesDegradation of nucleosome-associated centromeric histone H3-like protein CENP-A induced by herpes simplex virus type 1 protein ICP0Essential roles of Drosophila inner centromere protein (INCENP) and aurora B in histone H3 phosphorylation, metaphase chromosome alignment, kinetochore disjunction, and chromosome segregationProtein interaction domains of the ubiquitin-specific protease, USP7/HAUSPHSV-1 ICP0: paving the way for viral replicationA RING finger ubiquitin ligase is protected from autocatalyzed ubiquitination and degradation by binding to ubiquitin-specific protease USP7Posttranslational processing of infected cell proteins 0 and 4 of herpes simplex virus 1 is sequential and reflects the subcellular compartment in which the proteins localizeChk2 is required for HSV-1 ICP0-mediated G2/M arrest and enhancement of virus growthRole of chromatin during herpesvirus infections.ICP0 induces the accumulation of colocalizing conjugated ubiquitin.Comparison of the biological and biochemical activities of several members of the alphaherpesvirus ICP0 family of proteins.SUMO/sentrin: protein modifiers regulating important cellular functions.The 2 microm plasmid causes cell death in Saccharomyces cerevisiae with a mutation in Ulp1 protease.Perturbation of cell cycle progression and cellular gene expression as a function of herpes simplex virus ICP0.Truncation of the C-terminal acidic transcriptional activation domain of herpes simplex virus VP16 renders expression of the immediate-early genes almost entirely dependent on ICP0Efficient activation of viral genomes by levels of herpes simplex virus ICP0 insufficient to affect cellular gene expression or cell survival.Interactions of herpes simplex virus type 1 with ND10 and recruitment of PML to replication compartments.Requirements for the nuclear-cytoplasmic translocation of infected-cell protein 0 of herpes simplex virus 1Role of cyclin D3 in the biology of herpes simplex virus 1 ICPO.RING-H2 protein WSSV249 from white spot syndrome virus sequesters a shrimp ubiquitin-conjugating enzyme, PvUbc, for viral pathogenesisHSV-1 ICP0: An E3 Ubiquitin Ligase That Counteracts Host Intrinsic and Innate ImmunityExpression Profiling of WSSV ORF 199 and Shrimp Ubiquitin Conjugating Enzyme in WSSV Infected Penaeus monodonHerpes simplex virus 1-infected cell protein 0 contains two E3 ubiquitin ligase sites specific for different E2 ubiquitin-conjugating enzymesNovel roles of cytoplasmic ICP0: proteasome-independent functions of the RING finger are required to block interferon-stimulated gene production but not to promote viral replication.The intrinsic antiviral defense to incoming HSV-1 genomes includes specific DNA repair proteins and is counteracted by the viral protein ICP0.HSV-1-based vectors for gene therapy of neurological diseases and brain tumors: part I. HSV-1 structure, replication and pathogenesis.Recombinogenic telomeres in diploid Sorex granarius (Soricidae, Eulipotyphla) fibroblast cells.Herpes simplex virus 1 alpha regulatory protein ICP0 functionally interacts with cellular transcription factor BMAL1.
P2860
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P2860
Specific destruction of kinetochore protein CENP-C and disruption of cell division by herpes simplex virus immediate-early protein Vmw110.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Specific destruction of kineto ...... mmediate-early protein Vmw110.
@en
type
label
Specific destruction of kineto ...... mmediate-early protein Vmw110.
@en
prefLabel
Specific destruction of kineto ...... mmediate-early protein Vmw110.
@en
P2093
P2860
P356
P1433
P1476
Specific destruction of kineto ...... immediate-early protein Vmw110
@en
P2093
P2860
P304
P356
10.1093/EMBOJ/18.6.1526
P407
P577
1999-03-01T00:00:00Z