1x0n: Difference between revisions

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[[Image:1x0n.gif|left|200px]]<br /><applet load="1x0n" size="350" color="white" frame="true" align="right" spinBox="true"
[[Image:1x0n.gif|left|200px]]
caption="1x0n" />
 
'''NMR structure of growth factor receptor binding protein SH2 domain complexed with the inhibitor'''<br />
{{Structure
|PDB= 1x0n |SIZE=350|CAPTION= <scene name='initialview01'>1x0n</scene>
|SITE=  
|LIGAND= <scene name='pdbligand=DTF:4-[(10S,14S,18S)-18-(2-AMINO-2-OXOETHYL)-14-(1-NAPHTHYLMETHYL)-8,17,20-TRIOXO-7,16,19-TRIAZASPIRO[5.14]ICOS-11-EN-10-YL]BENZYLPHOSPHONIC ACID'>DTF</scene>
|ACTIVITY=
|GENE=
}}
 
'''NMR structure of growth factor receptor binding protein SH2 domain complexed with the inhibitor'''
 


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1X0N 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=DTF:'>DTF</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1X0N OCA].  
1X0N is a [[Single protein]] structure of sequence 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=1X0N OCA].  
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: peptide binding protein]]
[[Category: peptide binding protein]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:50:00 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 15:03:46 2008''

Revision as of 13:03, 20 March 2008

File:1x0n.gif


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1x0n
Ligands: DTF
Coordinates: save as pdb, mmCIF, xml



NMR structure of growth factor receptor binding protein SH2 domain complexed with the inhibitor


Disease

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

About this Structure

1X0N is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Thu Mar 20 15:03:46 2008

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