Evidence that the nuclease activities associated with the herpes simplex type 1 DNA polymerase are due to the 3'-5' exonuclease
Author:
Affiliation:
1. Department of Molecular and Cellular Biology, University of Arizona, Tucson, Arizona 85721, USA.
Abstract
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Link
https://journals.asm.org/doi/pdf/10.1128/jvi.70.7.4816-4818.1996
Reference11 articles.
1. A general structure for DNA-dependent DNA polymerases;Blanco L.;Gene,1991
2. Herpes simplex-1 DNA polymerase. Identification of an intrinsic 5~-3~ exonuclease with ribonuclease H activity;Crute J. J.;J. Biol. Chem.,1989
3. The herpes simplex virus type 1 UL42 gene product: a subunit of DNA polymerase that functions to increase processivity;Gottlieb J.;J. Virol.,1990
4. Mutations within conserved motifs in the 3~-5~ exonuclease domain of herpes simplex virus DNA polymerase;Hall J. D.;J. Gen. Virol.,1995
5. Knopf C. W. and R. Strick. 1994. Herpes simplex virus type 1 DNA polymerase: Eukaryotic model enzyme and principal target of antiviral therapy p. 87-135. In Y. Becker and G. Darai (ed.) Frontiers of virology vol. 3. Springer-Verlag Berlin.
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1. Herpesvirus DNA polymerase: Structures, functions, and mechanisms;Viral Replication Enzymes and their Inhibitors Part B;2021
2. Herpes Simplex Virus 1 DNA Polymerase RNase H Activity Acts in a 3′-to-5′ Direction and Is Dependent on the 3′-to-5′ Exonuclease Active Site;Journal of Virology;2018-03
3. On the role of proofreading exonuclease in bypass of a 1,2 d(GpG) cisplatin adduct by the herpes simplex virus-1 DNA polymerase;DNA Repair;2004-06
4. Herpes Simplex Virus Processivity Factor UL42 Imparts Increased DNA-Binding Specificity to the Viral DNA Polymerase and Decreased Dissociation from Primer-Template without Reducing the Elongation Rate;Journal of Virology;1999-01
5. DNA binding properties and processive proofreading of herpes simplex virus type 1 DNA polymerase;Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology;1998-11
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