3be9: Difference between revisions

Revision as of 08:40, 20 November 2008

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:3be9.jpg

Template:STRUCTURE 3be9

Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activitiesStructure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities

Template:ABSTRACT PUBMED 18055206

About this StructureAbout this Structure

3BE9 is a 1 chain structure of sequence from Zea mays. Full crystallographic information is available from OCA.

ReferenceReference

Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities., Nie Z, Perretta C, Erickson P, Margosiak S, Lu J, Averill A, Almassy R, Chu S, Bioorg Med Chem Lett. 2008 Jan 15;18(2):619-23. Epub 2007 Nov 28. PMID:18055206

Page seeded by OCA on Thu Nov 20 07:40:37 2008

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

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-'''Unreleased structure'''
+{{Seed}}
+[[Image:3be9.jpg|left|200px]]
-The entry 3be9 is ON HOLD  until Nov 16 2009
+<!--
+The line below this paragraph, containing "STRUCTURE_3be9", creates the "Structure Box" on the page.
+You may change the PDB parameter (which sets the PDB file loaded into the applet)
+or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
+or leave the SCENE parameter empty for the default display.
+-->
+{{STRUCTURE_3be9|  PDB=3be9  |  SCENE=  }}
-Authors: Nie, Z., Perretta, C., Erickson, P., Margosiak, S., Lu, J., Averill, A., Almassy, R., Chu, S.
+===Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities===
-Description: Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities
+<!--
+The line below this paragraph, {{ABSTRACT_PUBMED_18055206}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 18055206 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_18055206}}
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 11 09:25:33 2008''
+==About this Structure==
+BE9 is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Zea_mays Zea mays]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3BE9 OCA].
+==Reference==
+Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities., Nie Z, Perretta C, Erickson P, Margosiak S, Lu J, Averill A, Almassy R, Chu S, Bioorg Med Chem Lett. 2008 Jan 15;18(2):619-23. Epub 2007 Nov 28. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18055206 18055206]
+[[Category: Non-specific serine/threonine protein kinase]]
+[[Category: Zea mays]]
+[[Category: Almassy, R.]]
+[[Category: Averill, A.]]
+[[Category: Chu, S.]]
+[[Category: Erickson, P.]]
+[[Category: Lu, J.]]
+[[Category: Margosiak, S.]]
+[[Category: Nie, Z.]]
+[[Category: Perretta, C.]]
+[[Category: Atp-binding]]
+[[Category: Casein kinase ii]]
+[[Category: Enzyme-inhibitor complex]]
+[[Category: Nucleotide-binding]]
+[[Category: Protein kinase ck2]]
+[[Category: Serine/threonine-protein kinase]]
+[[Category: Structure-based drug design]]
+[[Category: Transferase]]
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Nov 20 07:40:37 2008''