1kim: Difference between revisions

New page: left|200px<br /><applet load="1kim" size="450" color="white" frame="true" align="right" spinBox="true" caption="1kim, resolution 2.14Å" /> '''CRYSTAL STRUCTURE OF...
 
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'''CRYSTAL STRUCTURE OF THYMIDINE KINASE FROM HERPES SIMPLEX VIRUS TYPE I COMPLEXED WITH DEOXYTHYMIDINE'''<br />
'''CRYSTAL STRUCTURE OF THYMIDINE KINASE FROM HERPES SIMPLEX VIRUS TYPE I COMPLEXED WITH DEOXYTHYMIDINE'''<br />


==Overview==
==Overview==
Antiherpes therapies are principally targeted at viral thymidine kinases, and utilize nucleoside analogs, the triphosphates of which are inhibitors, of viral DNA polymerase or result in toxic effects when incorporated into, DNA. The most frequently used drug, aciclovir (Zovirax), is a relatively, poor substrate for thymidine kinase and high-resolution structural, information on drugs and other molecules binding to the target is, therefore important for the design of novel and more potent chemotherapy, both in antiherpes treatment and in gene therapy systems where thymidine, kinase is expressed. Here, we report for the first time the binary, complexes of HSV-1 thymidine kinase (TK) with the drug molecules aciclovir, and penciclovir, determined by X-ray crystallography at 2.37 A resolution., Moreover, from new data at 2.14 A resolution, the refined structure of the, complex of TK with its substrate deoxythymidine (R = 0.209 for 96% of all, data) now reveals much detail concerning substrate and solvent, interactions with the enzyme. Structures of the complexes of TK with four, halogen-containing substrate analogs have also been solved, to resolutions, better than 2.4 A. The various TK inhibitors broadly fall into three, groups which together probe the space of the enzyme active site in a, manner that no one molecule does alone, so giving a composite picture of, active site interactions that can be exploited in the design of novel, compounds.
Antiherpes therapies are principally targeted at viral thymidine kinases and utilize nucleoside analogs, the triphosphates of which are inhibitors of viral DNA polymerase or result in toxic effects when incorporated into DNA. The most frequently used drug, aciclovir (Zovirax), is a relatively poor substrate for thymidine kinase and high-resolution structural information on drugs and other molecules binding to the target is therefore important for the design of novel and more potent chemotherapy, both in antiherpes treatment and in gene therapy systems where thymidine kinase is expressed. Here, we report for the first time the binary complexes of HSV-1 thymidine kinase (TK) with the drug molecules aciclovir and penciclovir, determined by X-ray crystallography at 2.37 A resolution. Moreover, from new data at 2.14 A resolution, the refined structure of the complex of TK with its substrate deoxythymidine (R = 0.209 for 96% of all data) now reveals much detail concerning substrate and solvent interactions with the enzyme. Structures of the complexes of TK with four halogen-containing substrate analogs have also been solved, to resolutions better than 2.4 A. The various TK inhibitors broadly fall into three groups which together probe the space of the enzyme active site in a manner that no one molecule does alone, so giving a composite picture of active site interactions that can be exploited in the design of novel compounds.


==About this Structure==
==About this Structure==
1KIM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Human_herpesvirus_4 Human herpesvirus 4] with SO4 and THM as [http://en.wikipedia.org/wiki/ligands ligands]. This structure superseeds the now removed PDB entry 1KIN. Active as [http://en.wikipedia.org/wiki/Thymidine_kinase Thymidine kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.21 2.7.1.21] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1KIM OCA].  
1KIM is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Human_herpesvirus_4 Human herpesvirus 4] with <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=THM:'>THM</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. This structure supersedes the now removed PDB entry 1KIN. Active as [http://en.wikipedia.org/wiki/Thymidine_kinase Thymidine kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.21 2.7.1.21] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1KIM OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Thymidine kinase]]
[[Category: Thymidine kinase]]
[[Category: Bennett, M.S.]]
[[Category: Bennett, M S.]]
[[Category: Brown, D.G.]]
[[Category: Brown, D G.]]
[[Category: Champness, J.N.]]
[[Category: Champness, J N.]]
[[Category: Davies, A.]]
[[Category: Davies, A.]]
[[Category: Melitz, C.]]
[[Category: Melitz, C.]]
[[Category: Rizkallah, P.J.]]
[[Category: Rizkallah, P J.]]
[[Category: Sanderson, M.R.]]
[[Category: Sanderson, M R.]]
[[Category: Sandhu, G.]]
[[Category: Sandhu, G.]]
[[Category: Summers, W.C.]]
[[Category: Summers, W C.]]
[[Category: Visse, R.]]
[[Category: Visse, R.]]
[[Category: Wien, F.]]
[[Category: Wien, F.]]
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[[Category: viridae]]
[[Category: viridae]]


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