3bhv

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[[Image:3bhv.jpg|left|200px]]
[[Image:3bhv.jpg|left|200px]]
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{{Structure
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<!--
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|PDB= 3bhv |SIZE=350|CAPTION= <scene name='initialview01'>3bhv</scene>, resolution 2.100&Aring;
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The line below this paragraph, containing "STRUCTURE_3bhv", creates the "Structure Box" on the page.
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|SITE= <scene name='pdbsite=AC1:Mg+Binding+Site+For+Residue+B+1'>AC1</scene>, <scene name='pdbsite=AC2:Mg+Binding+Site+For+Residue+D+2'>AC2</scene>, <scene name='pdbsite=AC3:Var+Binding+Site+For+Residue+A+299'>AC3</scene>, <scene name='pdbsite=AC4:Var+Binding+Site+For+Residue+C+299'>AC4</scene>, <scene name='pdbsite=AC5:Sgm+Binding+Site+For+Residue+B+2'>AC5</scene>, <scene name='pdbsite=AC6:Sgm+Binding+Site+For+Residue+B+3'>AC6</scene> and <scene name='pdbsite=AC7:Sgm+Binding+Site+For+Residue+D+1'>AC7</scene>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=SGM:MONOTHIOGLYCEROL'>SGM</scene>, <scene name='pdbligand=TPO:PHOSPHOTHREONINE'>TPO</scene>, <scene name='pdbligand=VAR:9-AMINO-5-(2-AMINOPYRIMIDIN-4-YL)PYRIDO[3&#39;,2&#39;&#58;4,5]PYRROLO[1,2-C]PYRIMIDIN-4-OL'>VAR</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Cyclin-dependent_kinase Cyclin-dependent kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.22 2.7.11.22] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE= CDK2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), CCNA2, CCNA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9913 Bos taurus])
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-->
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|DOMAIN=
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{{STRUCTURE_3bhv| PDB=3bhv | SCENE= }}
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|RELATEDENTRY=[[3bht|3BHT]], [[3bhu|3BHU]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3bhv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3bhv OCA], [http://www.ebi.ac.uk/pdbsum/3bhv PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=3bhv RCSB]</span>
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}}
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'''Structure of phosphorylated Thr160 CDK2/cyclin A in complex with the inhibitor variolin B'''
'''Structure of phosphorylated Thr160 CDK2/cyclin A in complex with the inhibitor variolin B'''
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[[Category: Morris, J C.]]
[[Category: Morris, J C.]]
[[Category: Valette, A.]]
[[Category: Valette, A.]]
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[[Category: atp-binding]]
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[[Category: Atp-binding]]
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[[Category: cell cycle]]
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[[Category: Cell cycle]]
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[[Category: cell division]]
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[[Category: Cell division]]
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[[Category: cyclin]]
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[[Category: Cyclin]]
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[[Category: mitosis]]
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[[Category: Mitosis]]
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[[Category: nucleotide-binding]]
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[[Category: Nucleotide-binding]]
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[[Category: phosphoprotein]]
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[[Category: Phosphoprotein]]
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[[Category: phosphorylation]]
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[[Category: Phosphorylation]]
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[[Category: polymorphism]]
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[[Category: Polymorphism]]
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[[Category: ser/thr protein kinase]]
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[[Category: Ser/thr protein kinase]]
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[[Category: serine/threonine-protein kinase]]
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[[Category: Serine/threonine-protein kinase]]
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[[Category: transferase]]
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[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 20:46:48 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 05:26:22 2008''
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Revision as of 17:46, 4 May 2008

Image:3bhv.jpg

Template:STRUCTURE 3bhv

Structure of phosphorylated Thr160 CDK2/cyclin A in complex with the inhibitor variolin B


Overview

Protein kinases represent promising anticancer drug targets. We describe here the meriolins, a new family of inhibitors of cyclin-dependent kinases (CDK). Meriolins represent a chemical structural hybrid between meridianins and variolins, two families of kinase inhibitors extracted from various marine invertebrates. Variolin B is currently in preclinical evaluation as an antitumor agent. A selectivity study done on 32 kinases showed that, compared with variolin B, meriolins display enhanced specificity toward CDKs, with marked potency on CDK2 and CDK9. The structures of pCDK2/cyclin A/variolin B and pCDK2/cyclin A/meriolin 3 complexes reveal that the two inhibitors bind within the ATP binding site of the kinase, but in different orientations. Meriolins display better antiproliferative and proapoptotic properties in human tumor cell cultures than their parent molecules, meridianins and variolins. Phosphorylation at CDK1, CDK4, and CDK9 sites on, respectively, protein phosphatase 1alpha, retinoblastoma protein, and RNA polymerase II is inhibited in neuroblastoma SH-SY5Y cells exposed to meriolins. Apoptosis triggered by meriolins is accompanied by rapid Mcl-1 down-regulation, cytochrome c release, and activation of caspases. Meriolin 3 potently inhibits tumor growth in two mouse xenograft cancer models, namely, Ewing's sarcoma and LS174T colorectal carcinoma. Meriolins thus constitute a new CDK inhibitory scaffold, with promising antitumor activity, derived from molecules initially isolated from marine organisms.

About this Structure

3BHV is a Protein complex structure of sequences from Bos taurus and Homo sapiens. Full crystallographic information is available from OCA.

Reference

Meriolins, a new class of cell death inducing kinase inhibitors with enhanced selectivity for cyclin-dependent kinases., Bettayeb K, Tirado OM, Marionneau-Lambot S, Ferandin Y, Lozach O, Morris JC, Mateo-Lozano S, Drueckes P, Schachtele C, Kubbutat MH, Liger F, Marquet B, Joseph B, Echalier A, Endicott JA, Notario V, Meijer L, Cancer Res. 2007 Sep 1;67(17):8325-34. PMID:17804748 Page seeded by OCA on Sun May 4 20:46:48 2008

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