C-terminal region of herpes simplex virus ICP8 protein needed for intranuclear localization (Q40646341)

22 September 2017

title

C-terminal region of herpes simplex virus ICP8 protein needed for intranuclear localization (English)

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22 September 2017

Travis J Taylor

1

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22 September 2017

David M Knipe

series ordinal

2

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22 September 2017

language of work or name

English

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publication date

1 May 2003

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22 September 2017

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22 September 2017

volume

309

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22 September 2017

issue

2

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22 September 2017

page(s)

219-231

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Disruption of PML subnuclear domains by the acidic IE1 protein of human cytomegalovirus is mediated through interaction with PML and may modulate a RING finger-dependent cryptic transactivator function of PML

22 September 2017

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The herpes simplex virus type-1 single-strand DNA-binding protein, ICP8, increases the processivity of the UL9 protein DNA helicase

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A dominant mutant form of the herpes simplex virus ICP8 protein decreases viral late gene transcription

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Comparison of the intranuclear distributions of herpes simplex virus proteins involved in various viral functions

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Genetic identification of a portion of the herpes simplex virus ICP8 protein required for DNA-binding

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The C-terminal third of UL42, a HSV-1 DNA replication protein, is dispensable for viral growth.

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The UL8 subunit of the herpes simplex virus type-1 DNA helicase-primase optimizes utilization of DNA templates covered by the homologous single-strand DNA-binding protein ICP8.

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7 January 2021

The intranuclear location of a herpes simplex virus DNA-binding protein is determined by the status of viral DNA replication

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Identifiers

DOI

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22 September 2017

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