1cj1: Difference between revisions

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New page: left|200px<br /> <applet load="1cj1" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cj1, resolution 3.0Å" /> '''GROWTH FACTOR RECEPT...
 
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[[Image:1cj1.gif|left|200px]]<br />
[[Image:1cj1.gif|left|200px]]<br /><applet load="1cj1" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1cj1" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1cj1, resolution 3.0&Aring;" />
caption="1cj1, resolution 3.0&Aring;" />
'''GROWTH FACTOR RECEPTOR BINDING PROTEIN SH2 DOMAIN (HUMAN) COMPLEXED WITH A PHOSPHOTYROSYL DERIVATIVE'''<br />
'''GROWTH FACTOR RECEPTOR BINDING PROTEIN SH2 DOMAIN (HUMAN) COMPLEXED WITH A PHOSPHOTYROSYL DERIVATIVE'''<br />


==Overview==
==Overview==
Previous efforts in the search for molecules capable of blocking the, associations between the activated tyrosine kinase growth factor receptors, and the SH2 domain of Grb2 had resulted in the identification of, 3-amino-Z-pTyr-Ac6c-Asn-NH2, a high-affinity and selective antagonist of, this SH2 domain. In the present paper, we report the successful, replacement of asparagine in this compound by a beta-amino acid mimetic, which brings us closer to our objective of identifying a Grb2-SH2, antagonist suitable for pharmacological investigations.
Previous efforts in the search for molecules capable of blocking the associations between the activated tyrosine kinase growth factor receptors and the SH2 domain of Grb2 had resulted in the identification of 3-amino-Z-pTyr-Ac6c-Asn-NH2, a high-affinity and selective antagonist of this SH2 domain. In the present paper, we report the successful replacement of asparagine in this compound by a beta-amino acid mimetic, which brings us closer to our objective of identifying a Grb2-SH2 antagonist suitable for pharmacological investigations.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1CJ1 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with C78 as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1CJ1 OCA].  
1CJ1 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=C78:'>C78</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CJ1 OCA].  


==Reference==
==Reference==
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[[Category: signal transduction]]
[[Category: signal transduction]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:06:43 2008''

Revision as of 13:06, 21 February 2008

File:1cj1.gif


1cj1, resolution 3.0Å

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GROWTH FACTOR RECEPTOR BINDING PROTEIN SH2 DOMAIN (HUMAN) COMPLEXED WITH A PHOSPHOTYROSYL DERIVATIVE

OverviewOverview

Previous efforts in the search for molecules capable of blocking the associations between the activated tyrosine kinase growth factor receptors and the SH2 domain of Grb2 had resulted in the identification of 3-amino-Z-pTyr-Ac6c-Asn-NH2, a high-affinity and selective antagonist of this SH2 domain. In the present paper, we report the successful replacement of asparagine in this compound by a beta-amino acid mimetic, which brings us closer to our objective of identifying a Grb2-SH2 antagonist suitable for pharmacological investigations.

DiseaseDisease

Known diseases associated with this structure: Central hypoventilation syndrome, congenital OMIM:[100790], Haddad syndrome OMIM:[100790]

About this StructureAbout this Structure

1CJ1 is a Single protein structure of sequence from Homo sapiens with as ligand. Full crystallographic information is available from OCA.

ReferenceReference

Structure-based design, synthesis, and X-ray crystallography of a high-affinity antagonist of the Grb2-SH2 domain containing an asparagine mimetic., Furet P, Garcia-Echeverria C, Gay B, Schoepfer J, Zeller M, Rahuel J, J Med Chem. 1999 Jul 1;42(13):2358-63. PMID:10395476

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