Foamy virus capsid assembly occurs at a pericentriolar region through a cytoplasmic targeting/retention signal in Gag.
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The DEAD-box RNA helicase DDX6 is required for efficient encapsidation of a retroviral genomeFoamy virus assembly with emphasis on pol encapsidationFoamy virus biology and its application for vector developmentFoamy virus budding and releaseNuclear trafficking of retroviral RNAs and Gag proteins during late steps of replicationCryo-electron Microscopy Structure of the Native Prototype Foamy Virus Glycoprotein and Virus ArchitectureHIV-1 and M-PMV RNA Nuclear Export Elements Program Viral Genomes for Distinct Cytoplasmic Trafficking Behaviors.A unique spumavirus Gag N-terminal domain with functional properties of orthoretroviral matrix and capsidTy3 capsid mutations reveal early and late functions of the amino-terminal domainFoamy Virus Protein-Nucleic Acid Interactions during Particle MorphogenesisAn N-terminal domain helical motif of Prototype Foamy Virus Gag with dual functions essential for particle egress and viral infectivityDrosophila errantivirusesCentrosomal latency of incoming foamy viruses in resting cells.Structural basis for spumavirus GAG tethering to chromatinInvestigating the intercellular spreading properties of the foamy virus Gag protein.A nuclear export signal within the structural Gag protein is required for prototype foamy virus replicationPericentriolar Targeting of the Mouse Mammary Tumor Virus GAG Protein.Structure of a Spumaretrovirus Gag Central Domain Reveals an Ancient Retroviral Capsid.Ty3 nucleocapsid controls localization of particle assemblyMutations in the amino terminus of foamy virus Gag disrupt morphology and infectivity but do not target assembly.Centrosome and retroviruses: the dangerous liaisons.More than one door - Budding of enveloped viruses through cellular membranes.P bodies, stress granules, and viral life cycles.Mutagenesis of N-terminal residues of feline foamy virus Gag reveals entirely distinct functions during capsid formation, particle assembly, Gag processing and budding.Molecular biology of foamy viruses.The foamy virus Gag proteins: what makes them different?Orthoretroviral-like prototype foamy virus Gag-Pol expression is compatible with viral replication.Prototype foamy virus protease activity is essential for intraparticle reverse transcription initiation but not absolutely required for uncoating upon host cell entry.A small-molecule-controlled system for efficient pseudotyping of prototype foamy virus vectorsMicrotubule Regulation and Function during Virus Infection.N-terminally myristoylated feline foamy virus Gag allows Env-independent budding of sub-viral particles.Analysis of prototype foamy virus particle-host cell interaction with autofluorescent retroviral particles.The C terminus of foamy retrovirus Gag contains determinants for encapsidation of Pol protein into virions.Subviral particle release determinants of prototype foamy virus.Foamy virus Pol protein expressed as a Gag-Pol fusion retains enzymatic activities, allowing for infectious virus productionEpstein-Barr virus thymidine kinase is a centrosomal resident precisely localized to the periphery of centrioles.Characterization and manipulation of foamy virus membrane interactions.
P2860
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P2860
Foamy virus capsid assembly occurs at a pericentriolar region through a cytoplasmic targeting/retention signal in Gag.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Foamy virus capsid assembly oc ...... eting/retention signal in Gag.
@en
type
label
Foamy virus capsid assembly oc ...... eting/retention signal in Gag.
@en
prefLabel
Foamy virus capsid assembly oc ...... eting/retention signal in Gag.
@en
P2093
P2860
P1433
P1476
Foamy virus capsid assembly oc ...... eting/retention signal in Gag.
@en
P2093
Maxine L Linial
Scott W Eastman
Shuyuarn F Yu
P2860
P304
P356
10.1111/J.1600-0854.2006.00448.X
P577
2006-06-02T00:00:00Z