Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin. - Wikidata - wikimedia - TriplyDB

Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin.

Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin.

http://www.wikidata.org/entity/Q33793377

about

Possible active origin of replication in the double stranded extended form of the left terminus of LuIII and its implication on the replication model of the parvovirus.Circulating HMGB1 and RAGE as Clinical Biomarkers in Malignant and Autoimmune Diseases Complementary induction of immunogenic cell death by oncolytic parvovirus H-1PV and gemcitabine in pancreatic cancer Genome packaging sense is controlled by the efficiency of the nick site in the right-end replication origin of parvoviruses minute virus of mice and LuIII Initiation of minute virus of mice DNA replication is regulated at the level of origin unwinding by atypical protein kinase C phosphorylation of NS1.Minute virus of mice initiator protein NS1 and a host KDWK family transcription factor must form a precise ternary complex with origin DNA for nicking to occur.Detection of head-to-tail DNA sequences of human bocavirus in clinical samples Characterization of a novel porcine parvovirus tentatively designated PPV5.Tumor Selectivity of Oncolytic Parvoviruses: From in vitro and Animal Models to Cancer Patients.Replication initiator protein NS1 of the parvovirus minute virus of mice binds to modular divergent sites distributed throughout duplex viral DNA.Structures of minute virus of mice replication initiator protein N-terminal domain: Insights into DNA nicking and origin binding Human HMGB1 directly facilitates interactions between nucleotide excision repair proteins on triplex-directed psoralen interstrand crosslinks The genome of human parvovirus b19 can replicate in nonpermissive cells with the help of adenovirus genes and produces infectious virus.Analysis of cis and trans Requirements for DNA Replication at the Right-End Hairpin of the Human Bocavirus 1 Genome.Segregation of a single outboard left-end origin is essential for the viability of parvovirus minute virus of mice.Mutations in the C-terminus of HBoV NS1 affect the function of NP1.Bidirectional replication from an internal ori site of the linear N15 plasmid prophage.Construction and production of oncotropic vectors, derived from MVM(p), that share reduced sequence homology with helper plasmids.

P2860

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P2860

Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin.

http://www.wikidata.org/entity/Q33793377

description

2000 nî lūn-bûn

@nan

2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2000年の論文

@ja

2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

@wuu

name

Two widely spaced initiator bi ...... ng-hairpin replication origin.

@ast

Two widely spaced initiator bi ...... ng-hairpin replication origin.

@en

type

label

Two widely spaced initiator bi ...... ng-hairpin replication origin.

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Two widely spaced initiator bi ...... ng-hairpin replication origin.

@en

prefLabel

Two widely spaced initiator bi ...... ng-hairpin replication origin.

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Two widely spaced initiator bi ...... ng-hairpin replication origin.

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P1433

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P2860

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P356

JVI.74.3.1332-1341.2000

P1433

Journal of Virology

P1476

Two widely spaced initiator bi ...... ng-hairpin replication origin.

@en

P2093

J Christensen

http://www.w3.org/2001/XMLSchema#string

P Tattersall

http://www.w3.org/2001/XMLSchema#string

S F Cotmore

http://www.w3.org/2001/XMLSchema#string

P2860

Two new members of the emerging KDWK family of combinatorial transcription modulators bind as a heterodimer to flexibly spaced PuCGPy half-sites

HMG1 interacts with HOX proteins and enhances their DNA binding and transcriptional activation

High mobility group protein 2 functionally interacts with the POU domains of octamer transcription factors

Sequencing end-labeled DNA with base-specific chemical cleavages

Biochemical activities of minute virus of mice nonstructural protein NS1 are modulated In vitro by the phosphorylation state of the polypeptide

High-mobility group 1/2 proteins are essential for initiating rolling-circle-type DNA replication at a parvovirus hairpin origin.

High mobility group chromosomal protein 1 binds to the adeno-associated virus replication protein (Rep) and promotes Rep-mediated site-specific cleavage of DNA, ATPase activity and transcriptional repression.

The minute virus of mice (MVM) nonstructural protein NS1 induces nicking of MVM DNA at a unique site of the right-end telomere in both hairpin and duplex conformations in vitro.

The NS1 polypeptide of the murine parvovirus minute virus of mice binds to DNA sequences containing the motif [ACCA]2-3

Minute virus of mice transcriptional activator protein NS1 binds directly to the transactivation region of the viral P38 promoter in a strictly ATP-dependent manner.

P304

1332-1341

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scholarly article

P356

10.1128/JVI.74.3.1332-1341.2000

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3

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74

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2000-02-01T00:00:00Z

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12685889

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10627544

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111468

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