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1l8c

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{{STRUCTURE_1l8c| PDB=1l8c | SCENE= }}
{{STRUCTURE_1l8c| PDB=1l8c | SCENE= }}
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'''STRUCTURAL BASIS FOR HIF-1ALPHA/CBP RECOGNITION IN THE CELLULAR HYPOXIC RESPONSE'''
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===STRUCTURAL BASIS FOR HIF-1ALPHA/CBP RECOGNITION IN THE CELLULAR HYPOXIC RESPONSE===
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==Overview==
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The cellular response to low tissue oxygen concentrations is mediated by the hypoxia-inducible transcription factor HIF-1. Under hypoxic conditions, HIF-1 activates transcription of critical adaptive genes by recruitment of the general coactivators CBP/p300 through interactions with its alpha-subunit (Hif-1 alpha). Disruption of the Hif-1 alpha/p300 interaction has been linked to attenuation of tumor growth. To delineate the structural basis for this interaction, we have determined the solution structure of the complex between the carboxy-terminal activation domain (CAD) of Hif-1 alpha and the zinc-binding TAZ1 (CH1) motif of cyclic-AMP response element binding protein (CREB) binding protein (CBP). Despite the overall similarity of the TAZ1 structure to that of the TAZ2 (part of the CH3) domain of CBP, differences occur in the packing of helices that can account for differences in specificity. The unbound CAD is intrinsically disordered and remains relatively extended upon binding, wrapping almost entirely around the TAZ1 domain in a groove through much of its surface. Three short helices are formed upon binding, stabilized by intermolecular interactions. The Asn-803 side chain, which functions as a hypoxic switch, is located on the second of these helices and is buried in the molecular interface. The third helix of the Hif-1 alpha CAD docks in a deep hydrophobic groove in TAZ1, providing extensive intermolecular hydrophobic interactions that contribute to the stability of the complex. The structure of this complex provides new insights into the mechanism through which Hif-1 alpha recruits CBP/p300 in response to hypoxia.
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The line below this paragraph, {{ABSTRACT_PUBMED_11959977}}, adds the Publication Abstract to the page
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(as it appears on PubMed at http://www.pubmed.gov), where 11959977 is the PubMed ID number.
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{{ABSTRACT_PUBMED_11959977}}
==About this Structure==
==About this Structure==
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1L8C is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1L8C OCA].
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1L8C is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1L8C OCA].
==Reference==
==Reference==
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[[Category: Wright, P E.]]
[[Category: Wright, P E.]]
[[Category: Gene regulation]]
[[Category: Gene regulation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 23:39:35 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 2 11:55:57 2008''

Revision as of 08:55, 2 July 2008

Image:1l8c.png

Template:STRUCTURE 1l8c

STRUCTURAL BASIS FOR HIF-1ALPHA/CBP RECOGNITION IN THE CELLULAR HYPOXIC RESPONSE

Template:ABSTRACT PUBMED 11959977

About this Structure

1L8C is a Protein complex structure of sequences from Homo sapiens and Mus musculus. Full experimental information is available from OCA.

Reference

Structural basis for Hif-1 alpha /CBP recognition in the cellular hypoxic response., Dames SA, Martinez-Yamout M, De Guzman RN, Dyson HJ, Wright PE, Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5271-6. PMID:11959977

Page seeded by OCA on Wed Jul 2 11:55:57 2008

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