1jsp

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /> <applet load="1jsp" size="450" color="white" frame="true" align="right" spinBox="true" caption="1jsp" /> '''NMR Structure of CBP Bromodomain in complex...)
Line 1: Line 1:
-
[[Image:1jsp.gif|left|200px]]<br />
+
[[Image:1jsp.gif|left|200px]]<br /><applet load="1jsp" size="350" color="white" frame="true" align="right" spinBox="true"
-
<applet load="1jsp" size="450" color="white" frame="true" align="right" spinBox="true"
+
caption="1jsp" />
caption="1jsp" />
'''NMR Structure of CBP Bromodomain in complex with p53 peptide'''<br />
'''NMR Structure of CBP Bromodomain in complex with p53 peptide'''<br />
==Overview==
==Overview==
-
Lysine acetylation of the tumor suppressor protein p53 in response to a, wide variety of cellular stress signals is required for its activation as, a transcription factor that regulates cell cycle arrest, senescence, or, apoptosis. Here, we report that the conserved bromo-domain of the, transcriptional coactivator CBP (CREB binding protein) binds specifically, to p53 at the C-terminal acetylated lysine 382. This, bromodomain/acetyl-lysine binding is responsible for p53, acetylation-dependent coactivator recruitment after DNA damage, a step, essential for p53-induced transcriptional activation of the, cyclin-dependent kinase inhibitor p21 in G1 cell cycle arrest. We further, present the three-dimensional nuclear magnetic resonance structure of the, CBP bromodomain in complex with a lysine 382-acetylated p53 peptide. Using, structural and biochemical analyses, we define the molecular determinants, for the specificity of this molecular recognition.
+
Lysine acetylation of the tumor suppressor protein p53 in response to a wide variety of cellular stress signals is required for its activation as a transcription factor that regulates cell cycle arrest, senescence, or apoptosis. Here, we report that the conserved bromo-domain of the transcriptional coactivator CBP (CREB binding protein) binds specifically to p53 at the C-terminal acetylated lysine 382. This bromodomain/acetyl-lysine binding is responsible for p53 acetylation-dependent coactivator recruitment after DNA damage, a step essential for p53-induced transcriptional activation of the cyclin-dependent kinase inhibitor p21 in G1 cell cycle arrest. We further present the three-dimensional nuclear magnetic resonance structure of the CBP bromodomain in complex with a lysine 382-acetylated p53 peptide. Using structural and biochemical analyses, we define the molecular determinants for the specificity of this molecular recognition.
==Disease==
==Disease==
Line 11: Line 10:
==About this Structure==
==About this Structure==
-
1JSP is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1JSP OCA].
+
1JSP is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JSP OCA].
==Reference==
==Reference==
Line 21: Line 20:
[[Category: Yan, S.]]
[[Category: Yan, S.]]
[[Category: Zeng, L.]]
[[Category: Zeng, L.]]
-
[[Category: Zhou, M.M.]]
+
[[Category: Zhou, M M.]]
[[Category: bromodomain]]
[[Category: bromodomain]]
[[Category: cbp]]
[[Category: cbp]]
[[Category: nmr structure.]]
[[Category: nmr structure.]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 17:43:57 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:26:20 2008''

Revision as of 11:26, 21 February 2008


1jsp

Drag the structure with the mouse to rotate

NMR Structure of CBP Bromodomain in complex with p53 peptide

Contents

Overview

Lysine acetylation of the tumor suppressor protein p53 in response to a wide variety of cellular stress signals is required for its activation as a transcription factor that regulates cell cycle arrest, senescence, or apoptosis. Here, we report that the conserved bromo-domain of the transcriptional coactivator CBP (CREB binding protein) binds specifically to p53 at the C-terminal acetylated lysine 382. This bromodomain/acetyl-lysine binding is responsible for p53 acetylation-dependent coactivator recruitment after DNA damage, a step essential for p53-induced transcriptional activation of the cyclin-dependent kinase inhibitor p21 in G1 cell cycle arrest. We further present the three-dimensional nuclear magnetic resonance structure of the CBP bromodomain in complex with a lysine 382-acetylated p53 peptide. Using structural and biochemical analyses, we define the molecular determinants for the specificity of this molecular recognition.

Disease

Known diseases associated with this structure: Adrenal cortical carcinoma OMIM:[191170], Blue-cone monochromacy OMIM:[303900], Breast cancer OMIM:[191170], Colorblindness, protan OMIM:[303900], Colorectal cancer OMIM:[191170], Hepatocellular carcinoma OMIM:[191170], Histiocytoma OMIM:[191170], Li-Fraumeni syndrome OMIM:[191170], Multiple malignancy syndrome OMIM:[191170], Nasopharyngeal carcinoma OMIM:[191170], Osteosarcoma OMIM:[191170], Pancreatic cancer OMIM:[191170], Rubenstein-Taybi syndrome OMIM:[600140], Thyroid carcinoma OMIM:[191170]

About this Structure

1JSP is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structural mechanism of the bromodomain of the coactivator CBP in p53 transcriptional activation., Mujtaba S, He Y, Zeng L, Yan S, Plotnikova O, Sachchidanand, Sanchez R, Zeleznik-Le NJ, Ronai Z, Zhou MM, Mol Cell. 2004 Jan 30;13(2):251-63. PMID:14759370

Page seeded by OCA on Thu Feb 21 13:26:20 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools