2d82

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
[[Image:2d82.gif|left|200px]]
[[Image:2d82.gif|left|200px]]
-
{{Structure
+
<!--
-
|PDB= 2d82 |SIZE=350|CAPTION= <scene name='initialview01'>2d82</scene>
+
The line below this paragraph, containing "STRUCTURE_2d82", 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=TTR:9-ACETYL-2,3,4,9-TETRAHYDRO-1H-CARBAZOL-1-ONE'>TTR</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/Histone_acetyltransferase Histone acetyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.48 2.3.1.48] </span>
+
or leave the SCENE parameter empty for the default display.
-
|GENE=
+
-->
-
|DOMAIN=
+
{{STRUCTURE_2d82| PDB=2d82 | SCENE= }}
-
|RELATEDENTRY=[[1jsp|1jsp]]
+
-
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2d82 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2d82 OCA], [http://www.ebi.ac.uk/pdbsum/2d82 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2d82 RCSB]</span>
+
-
}}
+
'''Target Structure-Based Discovery of Small Molecules that Block Human p53 and CREB Binding Protein (CBP) Association'''
'''Target Structure-Based Discovery of Small Molecules that Block Human p53 and CREB Binding Protein (CBP) Association'''
Line 35: Line 32:
[[Category: Zhou, M M.]]
[[Category: Zhou, M M.]]
[[Category: 9-acetyl-2,3,4,9-tetrahydro-carbazol-1-one]]
[[Category: 9-acetyl-2,3,4,9-tetrahydro-carbazol-1-one]]
-
[[Category: bromodomain]]
+
[[Category: Bromodomain]]
-
[[Category: cbp]]
+
[[Category: Cbp]]
-
[[Category: chemical ligand]]
+
[[Category: Chemical ligand]]
-
[[Category: creb]]
+
[[Category: Creb]]
-
[[Category: nmr structure]]
+
[[Category: Nmr structure]]
-
[[Category: p53]]
+
[[Category: P53]]
-
 
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 23:50:39 2008''
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:31:11 2008''
+

Revision as of 20:50, 3 May 2008

Template:STRUCTURE 2d82

Target Structure-Based Discovery of Small Molecules that Block Human p53 and CREB Binding Protein (CBP) Association


Overview

Lysine acetylation of human tumor suppressor p53 in response to cellular stress signals is required for its function as a transcription factor that regulates cell cycle arrest, senescence, or apoptosis. Here, we report small molecules that block lysine 382-acetylated p53 association with the bromodomain of the coactivator CBP, an interaction essential for p53-induced transcription of the cell cycle inhibitor p21 in response to DNA damage. These chemicals were discovered in target structure-guided nuclear magnetic resonance spectroscopy screening of a focused chemical library constructed based on the structural knowledge of CBP bromodomain/p53-AcK382 binding. Structural characterization shows that these chemicals inhibit CBP/p53 association by binding to the acetyl-lysine binding site of the bromodomain. Cell-based functional assays demonstrate that the lead chemicals can modulate p53 stability and function in response to DNA damage.

About this Structure

2D82 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Target structure-based discovery of small molecules that block human p53 and CREB binding protein association., Sachchidanand, Resnick-Silverman L, Yan S, Mutjaba S, Liu WJ, Zeng L, Manfredi JJ, Zhou MM, Chem Biol. 2006 Jan;13(1):81-90. PMID:16426974 Page seeded by OCA on Sat May 3 23:50:39 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools