Stable binding of the herpes simplex virus ICP47 protein to the peptide binding site of TAP
about
Viral inhibition of the transporter associated with antigen processing (TAP): a striking example of functional convergent evolutionVaricelloviruses avoid T cell recognition by UL49.5-mediated inactivation of the transporter associated with antigen processingThe human cytomegalovirus gene product US6 inhibits ATP binding by TAPVaricella-zoster virus retains major histocompatibility complex class I proteins in the Golgi compartment of infected cells.A negative feedback modulator of antigen processing evolved from a frameshift in the cowpox virus genome.Anterograde transport of herpes simplex virus capsids in neurons by both separate and married mechanismsVaricellovirus UL 49.5 proteins differentially affect the function of the transporter associated with antigen processing, TAP.Human cytomegalovirus UL18 utilizes US6 for evading the NK and T-cell responsesMechanisms of T-cell activation by human T-cell lymphotropic virus type I.A highly conserved sequence of the viral TAP inhibitor ICP47 is required for freezing of the peptide transport cycleInhibition of major histocompatibility complex class I antigen presentation in pig and primate cells by herpes simplex virus type 1 and 2 ICP47Expression of herpes simplex virus ICP47 and human cytomegalovirus US11 prevents recognition of transgene products by CD8(+) cytotoxic T lymphocytes.Site-directed mutagenesis of the virion host shutoff gene (UL41) of herpes simplex virus (HSV): analysis of functional differences between HSV type 1 (HSV-1) and HSV-2 alleles.Immature monocyte-derived dendritic cells are productively infected with herpes simplex virus type 1.Herpes simplex virus with highly reduced gD levels can efficiently enter and spread between human keratinocytes.Herpes simplex virus-specific memory CD8+ T cells are selectively activated and retained in latently infected sensory gangliaA human herpesvirus 7 glycoprotein, U21, diverts major histocompatibility complex class I molecules to lysosomesThe MHC class I antigen presentation pathway: strategies for viral immune evasion.Viral escape mechanisms--escapology taught by viruses.Major histocompatibility complex class I downregulation induced by equine herpesvirus type 1 pUL56 is through dynamin-dependent endocytosis.The capacity of UL49.5 proteins to inhibit TAP is widely distributed among members of the genus Varicellovirus.Immunization with herpes simplex virus 2 (HSV-2) genes plus inactivated HSV-2 is highly protective against acute and recurrent HSV-2 diseaseAllosteric crosstalk between peptide-binding, transport, and ATP hydrolysis of the ABC transporter TAPHerpes simplex virus glycoproteins gD and gE/gI serve essential but redundant functions during acquisition of the virion envelope in the cytoplasm.Experimental investigation of herpes simplex virus latencyEvasion of early antiviral responses by herpes simplex viruses.Localization, expression change in PRRSV infection and association analysis of the porcine TAP1 geneEfficient generation and rapid isolation via stoplight recombination of Herpes simplex viruses expressing model antigenic and immunological epitopes.Epstein-Barr viral BNLF2a protein hijacks the tail-anchored protein insertion machinery to block antigen processing by the transport complex TAP.Expression of gp19K increases the persistence of transgene expression from an adenovirus vector in the mouse lung and liver.CD8 T cell control of HSV reactivation from latency is abrogated by viral inhibition of MHC class IA CD8+ T cell immune evasion protein specific to Epstein-Barr virus and its close relatives in Old World primates.The human cytomegalovirus US6 glycoprotein inhibits transporter associated with antigen processing-dependent peptide translocation.Dancing with the enemy: the interplay of herpes simplex virus with dendritic cells.Herpes simplex virus type 1 infection of activated cytotoxic T cells: Induction of fratricide as a mechanism of viral immune evasionThe human immunodeficiency virus type 1 (HIV-1) Vpu protein interferes with an early step in the biosynthesis of major histocompatibility complex (MHC) class I molecules.The active site of ICP47, a herpes simplex virus-encoded inhibitor of the major histocompatibility complex (MHC)-encoded peptide transporter associated with antigen processing (TAP), maps to the NH2-terminal 35 residuesIntroduction of a glycosylation site into a secreted protein provides evidence for an alternative antigen processing pathway: transport of precursors of major histocompatibility complex class I-restricted peptides from the endoplasmic reticulum to tInfected cell protein (ICP)47 enhances herpes simplex virus neurovirulence by blocking the CD8+ T cell response.CD8(+) T cells can block herpes simplex virus type 1 (HSV-1) reactivation from latency in sensory neurons.
P2860
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P2860
Stable binding of the herpes simplex virus ICP47 protein to the peptide binding site of TAP
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Stable binding of the herpes s ...... he peptide binding site of TAP
@ast
Stable binding of the herpes s ...... he peptide binding site of TAP
@en
type
label
Stable binding of the herpes s ...... he peptide binding site of TAP
@ast
Stable binding of the herpes s ...... he peptide binding site of TAP
@en
prefLabel
Stable binding of the herpes s ...... he peptide binding site of TAP
@ast
Stable binding of the herpes s ...... he peptide binding site of TAP
@en
P2093
P2860
P1433
P1476
Stable binding of the herpes s ...... he peptide binding site of TAP
@en
P2093
Andrews DW
Johnson DC
van Endert P
P2860
P304
P407
P577
1996-07-01T00:00:00Z