Hepadnavirus reverse transcription initiates within the stem-loop of the RNA packaging signal and employs a novel strand transfer.
about
Identification and characterization of avihepadnaviruses isolated from exotic anseriformes maintained in captivityHepatitis B virus replicationSequence- and structure-specific determinants in the interaction between the RNA encapsidation signal and reverse transcriptase of avian hepatitis B virusesThermodynamics and NMR studies on Duck, Heron and Human HBV encapsidation signalsCharacterization of the intracellular deproteinized relaxed circular DNA of hepatitis B virus: an intermediate of covalently closed circular DNA formationEvidence that the RNAseH activity of the duck hepatitis B virus is unable to act on exogenous substratesHepatitis B virus reverse transcriptase: diverse functions as classical and emerging targets for antiviral interventionA bulged region of the hepatitis B virus RNA encapsidation signal contains the replication origin for discontinuous first-strand DNA synthesisNucleic acid chaperone activity associated with the arginine-rich domain of human hepatitis B virus core protein.Effects of genomic length on translocation of hepatitis B virus polymerase-linked oligomer.Properties of monoclonal antibodies directed against hepatitis B virus polymerase protein.Mapping of the hepatitis B virus reverse transcriptase TP and RT domains by transcomplementation for nucleotide priming and by protein-protein interactionGeneration of replication-competent hepatitis B virus nucleocapsids in insect cells.The duck hepatitis B virus polymerase is activated by its RNA packaging signal, epsilon.Interaction between hepatitis B virus core protein and reverse transcriptase.Serine phosphoacceptor sites within the core protein of hepatitis B virus contribute to genome replication pleiotropically.Human hepatitis B virus polymerase interacts with the molecular chaperonin Hsp60.Reconstitution of a functional duck hepatitis B virus replication initiation complex from separate reverse transcriptase domains expressed in Escherichia coliThe majority of duck hepatitis B virus reverse transcriptase in cells is nonencapsidated and is bound to a cytoplasmic structure.Hepadnavirus assembly and reverse transcription require a multi-component chaperone complex which is incorporated into nucleocapsids.Interferon prevents formation of replication-competent hepatitis B virus RNA-containing nucleocapsids.Identification of an essential molecular contact point on the duck hepatitis B virus reverse transcriptasePhosphoacceptors threonine 162 and serines 170 and 178 within the carboxyl-terminal RRRS/T motif of the hepatitis B virus core protein make multiple contributions to hepatitis B virus replication.A novel cis-acting element facilitates minus-strand DNA synthesis during reverse transcription of the hepatitis B virus genome.Distinct requirement for two stages of protein-primed initiation of reverse transcription in hepadnaviruses.Characterization of the host factors required for hepadnavirus covalently closed circular (ccc) DNA formationHepatitis B virus reverse transcriptase and epsilon RNA sequences required for specific interaction in vitro.Base pairing between the 5' half of epsilon and a cis-acting sequence, phi, makes a contribution to the synthesis of minus-strand DNA for human hepatitis B virus.Base pairing among three cis-acting sequences contributes to template switching during hepadnavirus reverse transcription.Heat shock protein 90-independent activation of truncated hepadnavirus reverse transcriptase.Evidence for multiple distinct interactions between hepatitis B virus P protein and its cognate RNA encapsidation signal during initiation of reverse transcription.Alpha-interferon suppresses hepadnavirus transcription by altering epigenetic modification of cccDNA minichromosomescis-Acting sequences 5E, M, and 3E interact to contribute to primer translocation and circularization during reverse transcription of avian hepadnavirus DNACombining genetic and biochemical approaches to identify functional molecular contact points.RNA elements directing translation of the duck hepatitis B Virus polymerase via ribosomal shunting.Three novel cis-acting elements required for efficient plus-strand DNA synthesis of the hepatitis B virus genome.Solution structure of the apical stem-loop of the human hepatitis B virus encapsidation signal.Cryptic protein priming sites in two different domains of duck hepatitis B virus reverse transcriptase for initiating DNA synthesis in vitro.Complementarity between epsilon and phi sequences in pregenomic RNA influences hepatitis B virus replication efficiency.Hepadnavirus Genome Replication and Persistence.
P2860
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P2860
Hepadnavirus reverse transcription initiates within the stem-loop of the RNA packaging signal and employs a novel strand transfer.
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
Hepadnavirus reverse transcrip ...... ploys a novel strand transfer.
@ast
Hepadnavirus reverse transcrip ...... ploys a novel strand transfer.
@en
type
label
Hepadnavirus reverse transcrip ...... ploys a novel strand transfer.
@ast
Hepadnavirus reverse transcrip ...... ploys a novel strand transfer.
@en
prefLabel
Hepadnavirus reverse transcrip ...... ploys a novel strand transfer.
@ast
Hepadnavirus reverse transcrip ...... ploys a novel strand transfer.
@en
P2093
P2860
P1433
P1476
Hepadnavirus reverse transcrip ...... mploys a novel strand transfer
@en
P2093
P2860
P304
P407
P50
P577
1994-06-01T00:00:00Z