Expression of functional hepatitis B virus polymerase in yeast reveals it to be the sole viral protein required for correct initiation of reverse transcription.
about
An in vivo assay for the reverse transcriptase of human retrotransposon L1 in Saccharomyces cerevisiaeSequence- and structure-specific determinants in the interaction between the RNA encapsidation signal and reverse transcriptase of avian hepatitis B virusesEvidence that the RNAseH activity of the duck hepatitis B virus is unable to act on exogenous substratesThe Molecular and Structural Basis of HBV-resistance to Nucleos(t)ide AnalogsThe hepatitis B virus ribonuclease H is sensitive to inhibitors of the human immunodeficiency virus ribonuclease H and integrase enzymesA bulged region of the hepatitis B virus RNA encapsidation signal contains the replication origin for discontinuous first-strand DNA synthesisProperties 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.Human hepatitis B virus polymerase interacts with the molecular chaperonin Hsp60.Hepatitis B virus biology.The majority of duck hepatitis B virus reverse transcriptase in cells is nonencapsidated and is bound to a cytoplasmic structure.Identification of an essential molecular contact point on the duck hepatitis B virus reverse transcriptaseThe yeast retrotransposon Ty5 uses the anticodon stem-loop of the initiator methionine tRNA as a primer for reverse transcription.Structure and function of the encapsidation signal of hepadnaviridae.Mutations in the epsilon sequences of human hepatitis B virus affect both RNA encapsidation and reverse transcriptionRNA sequences controlling the initiation and transfer of duck hepatitis B virus minus-strand DNA.Nucleotide priming and reverse transcriptase activity of hepatitis B virus polymerase expressed in insect cellsDetection of an RNase H activity associated with hepadnaviruses.Transcomplementation of nucleotide priming and reverse transcription between independently expressed TP and RT domains of the hepatitis B virus reverse transcriptase.In vitro epsilon RNA-dependent protein priming activity of human hepatitis B virus polymerase.TP-RT domain interactions of duck hepatitis B virus reverse transcriptase in cis and in trans during protein-primed initiation of DNA synthesis in vitro.Hepadnavirus reverse transcription initiates within the stem-loop of the RNA packaging signal and employs a novel strand transfer.Detection of DNA polymerase activities associated with purified duck hepatitis B virus core particles by using an activity gel assayReplication infidelity during a single cycle of Ty1 retrotransposition.Duck hepatitis B virus nucleocapsids formed by N-terminally extended or C-terminally truncated core proteins disintegrate during viral DNA maturation.Specific hepatitis B virus minus-strand DNA synthesis requires only the 5' encapsidation signal and the 3'-proximal direct repeat DR1.Evidence for activation of the hepatitis B virus polymerase by binding of its RNA template.Insertions within epsilon affect synthesis of minus-strand DNA before the template switch for duck hepatitis B virusSelected mutations of the duck hepatitis B virus P gene RNase H domain affect both RNA packaging and priming of minus-strand DNA synthesis.Effect of core protein phosphorylation by protein kinase C on encapsidation of RNA within core particles of hepatitis B virus.Priming of duck hepatitis B virus reverse transcription in vitro: premature termination of primer DNA induced by the 5'-triphosphate of fialuridine.Distinct requirements for primary sequence in the 5'- and 3'-part of a bulge in the hepatitis B virus RNA encapsidation signal revealed by a combined in vivo selection/in vitro amplification system.Efficient hammerhead ribozyme-mediated cleavage of the structured hepatitis B virus encapsidation signal in vitro and in cell extracts, but not in intact cells.Hepatitis B virus replication--an update.The arginine clusters of the carboxy-terminal domain of the core protein of hepatitis B virus make pleiotropic contributions to genome replication.Expression of hepatitis B virus polymerase in Ty1-his3AI retroelement of Saccharomyces cerevisiae.Expression of an enzymatically active polymerase of human hepatitis B virus in an coupled transcription-translation system.
P2860
Q24611767-F6EAFDCD-F944-4A65-B649-D2500F589202Q24673641-78EACC61-9316-4AFB-93CF-C129AC0DADF1Q24802171-A28CB6C2-7AFE-4F5F-B6A8-079F2173AA7EQ26781795-B7C284C2-C127-470E-BCE8-B5B5EE35A1CAQ28485228-F21A5D1E-65D1-40F4-A918-64BB0CE3AE66Q28775714-E2BAA1C4-28DA-4432-BB8C-F35A6B763F0AQ33647709-43731479-09F6-4CD2-AA80-0C1D1F084ED8Q33652843-44AE36A7-CD5D-4056-B167-6FBECF8418B0Q33783031-2FBB4D99-80C9-423A-9714-348572BA1B7FQ33785615-C757365E-6A7E-4C63-8E68-E2893941CD4EQ33844349-8AE86730-26EC-44A5-A3DA-9813992277BFQ33855246-F955DED7-2942-4847-84DF-50B735E60681Q33874395-143279C1-A243-430F-94B7-C3D80A7991DBQ33911921-6F7C2813-ED95-4998-8D81-E9DCF3B0018EQ34361988-98593D43-3DF9-4A40-A4F1-5EEF48266ABDQ34484008-13CDAE3F-149A-4AF6-989C-607BAAB00092Q35839084-1DB5DEE9-4F03-41FB-8213-B33EEBFD358AQ35841519-23844359-F483-4297-ABDB-6626014386CCQ35841847-51D32C2B-C07D-4EF4-A57E-83C63AB303DDQ35845946-09F99DB3-26B5-4073-B231-89F63194608FQ35880961-FEB11D27-9388-4F4F-B616-41E16270B3C4Q35943827-28115658-5C0E-418D-813B-0C6301E6686EQ36086752-459A96FA-1FAD-4EDD-BBBC-F5B9D8C28C8FQ36634003-141441A0-9AA3-4B0F-8739-41BB7C90FAA3Q36654330-E8981335-8E97-4E07-9D9A-905AE8C8FCECQ37439115-9FB88A8C-C612-4831-A5F8-FB70606C5BF0Q39582132-82983441-D91B-421C-BAA9-BE8C344177CCQ39873190-497A7DB4-092D-43DA-ABCB-2C5C3E47B882Q39875943-B3B8DE57-8CAF-477D-9BBF-986D367A0E5FQ39880270-102A8131-DAF1-48B5-A33E-E93C0C12060AQ40038621-545DD13E-2A55-46FE-AECC-06BAFF5660E5Q40042957-E911B2F4-794D-419F-B52F-7F951D2ED37EQ40043127-15FB5FF3-FDDD-4E6A-9F31-73112B467351Q40396119-00BA3717-0937-4702-8354-559EFD1364EDQ40397070-1C79A3A7-D9DC-468B-9672-90EDE664F025Q41207104-63F65769-EFA5-4B46-A299-ADC33CACF8F6Q42170017-BC7BA4AA-31B0-419D-B188-53D809EE5A16Q45746657-26BF68B3-E28C-488C-8834-6DBF11664923Q45748007-EA957D78-0BC9-48B7-9FA0-BF0C23EF683C
P2860
Expression of functional hepatitis B virus polymerase in yeast reveals it to be the sole viral protein required for correct initiation of reverse transcription.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh
1993年學術文章
@zh-hant
name
Expression of functional hepat ...... tion of reverse transcription.
@ast
Expression of functional hepat ...... tion of reverse transcription.
@en
type
label
Expression of functional hepat ...... tion of reverse transcription.
@ast
Expression of functional hepat ...... tion of reverse transcription.
@en
prefLabel
Expression of functional hepat ...... tion of reverse transcription.
@ast
Expression of functional hepat ...... tion of reverse transcription.
@en
P2860
P356
P1476
Expression of functional hepat ...... tion of reverse transcription.
@en
P2093
P2860
P304
P356
10.1073/PNAS.90.9.4107
P407
P50
P577
1993-05-01T00:00:00Z