2gv9: Difference between revisions

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[[Image:2gv9.gif|left|200px]]
[[Image:2gv9.gif|left|200px]]


{{Structure
<!--
|PDB= 2gv9 |SIZE=350|CAPTION= <scene name='initialview01'>2gv9</scene>, resolution 2.68&Aring;
The line below this paragraph, containing "STRUCTURE_2gv9", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=GAI:GUANIDINE'>GAI</scene>, <scene name='pdbligand=HG:MERCURY+(II)+ION'>HG</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/DNA-directed_DNA_polymerase DNA-directed DNA polymerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.7.7 2.7.7.7] </span>
or leave the SCENE parameter empty for the default display.
|GENE= UL30 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10298 Human herpesvirus 1])
-->
|DOMAIN=
{{STRUCTURE_2gv9| PDB=2gv9  | SCENE= }}  
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2gv9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2gv9 OCA], [http://www.ebi.ac.uk/pdbsum/2gv9 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2gv9 RCSB]</span>
}}


'''Crystal structure of the Herpes Simplex virus type 1 DNA polymerase'''
'''Crystal structure of the Herpes Simplex virus type 1 DNA polymerase'''
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Liu, S.]]
[[Category: Liu, S.]]
[[Category: polymerase alpha fold]]
[[Category: Polymerase alpha fold]]
 
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Revision as of 05:34, 4 May 2008

File:2gv9.gif

Template:STRUCTURE 2gv9

Crystal structure of the Herpes Simplex virus type 1 DNA polymerase


OverviewOverview

Herpesviruses are the second leading cause of human viral diseases. Herpes Simplex Virus types 1 and 2 and Varicella-zoster virus produce neurotropic infections such as cutaneous and genital herpes, chickenpox, and shingles. Infections of a lymphotropic nature are caused by cytomegalovirus, HSV-6, HSV-7, and Epstein-Barr virus producing lymphoma, carcinoma, and congenital abnormalities. Yet another series of serious health problems are posed by infections in immunocompromised individuals. Common therapies for herpes viral infections employ nucleoside analogs, such as Acyclovir, and target the viral DNA polymerase, essential for viral DNA replication. Although clinically useful, this class of drugs exhibits a narrow antiviral spectrum, and resistance to these agents is an emerging problem for disease management. A better understanding of herpes virus replication will help the development of new safe and effective broad spectrum anti-herpetic drugs that fill an unmet need. Here, we present the first crystal structure of a herpesvirus polymerase, the Herpes Simplex Virus type 1 DNA polymerase, at 2.7 A resolution. The structural similarity of this polymerase to other alpha polymerases has allowed us to construct high confidence models of a replication complex of the polymerase and of Acyclovir as a DNA chain terminator. We propose a novel inhibition mechanism in which a representative of a series of non-nucleosidic viral polymerase inhibitors, the 4-oxo-dihydroquinolines, binds at the polymerase active site interacting non-covalently with both the polymerase and the DNA duplex.

About this StructureAbout this Structure

2GV9 is a Single protein structure of sequence from Human herpesvirus 1. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure of the herpes simplex virus 1 DNA polymerase., Liu S, Knafels JD, Chang JS, Waszak GA, Baldwin ET, Deibel MR Jr, Thomsen DR, Homa FL, Wells PA, Tory MC, Poorman RA, Gao H, Qiu X, Seddon AP, J Biol Chem. 2006 Jun 30;281(26):18193-200. Epub 2006 Apr 24. PMID:16638752 Page seeded by OCA on Sun May 4 05:34:51 2008

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