1skj: Difference between revisions

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|PDB= 1skj |SIZE=350|CAPTION= <scene name='initialview01'>1skj</scene>, resolution 2.0&Aring;
|PDB= 1skj |SIZE=350|CAPTION= <scene name='initialview01'>1skj</scene>, resolution 2.0&Aring;
|SITE=  
|SITE=  
|LIGAND= <scene name='pdbligand=UR2:4-[3-CARBOXYMETHYL-3-(4-PHOSPHONOOXY-BENZYL)-UREIDO]-4-[(3-CYCLOHEXYL-PROPYL)-METHYL-CARBAMOYL]BUTYRIC ACID'>UR2</scene>
|LIGAND= <scene name='pdbligand=UR2:4-[3-CARBOXYMETHYL-3-(4-PHOSPHONOOXY-BENZYL)-UREIDO]-4-[(3-CYCLOHEXYL-PROPYL)-METHYL-CARBAMOYL]BUTYRIC+ACID'>UR2</scene>
|ACTIVITY= [http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 and 2.7.10.2 2.7.10.1 and 2.7.10.2]  
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 and 2.7.10.2 2.7.10.1 and 2.7.10.2] </span>
|GENE=  
|GENE=  
|DOMAIN=
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1skj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1skj OCA], [http://www.ebi.ac.uk/pdbsum/1skj PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1skj RCSB]</span>
}}
}}


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[[Category: Holland, D R.]]
[[Category: Holland, D R.]]
[[Category: Rubin, J R.]]
[[Category: Rubin, J R.]]
[[Category: UR2]]
[[Category: peptidomimetic]]
[[Category: peptidomimetic]]
[[Category: phosphotyrosine recognition domain]]
[[Category: phosphotyrosine recognition domain]]
Line 33: Line 35:
[[Category: v-src sh2 domain]]
[[Category: v-src sh2 domain]]


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Revision as of 20:43, 30 March 2008

File:1skj.gif


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1skj, resolution 2.0Å
Ligands: UR2
Activity: Transferase, with EC number and 2.7.10.2 2.7.10.1 and 2.7.10.2
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



COCRYSTAL STRUCTURE OF UREA-SUBSTITUTED PHOSPHOPEPTIDE COMPLEX


Overview

The specific association of an SH2 domain with a phosphotyrosine (pTyr)-containing sequence of another protein precipitates a cascade of intracellular molecular interactions (signals) which effect a wide range of intracellular processes. The nonreceptor tyrosine kinase Src, which has been associated with breast cancer and osteoporosis, contains an SH2 domain. Inhibition of Src SH2-phosphoprotein interactions by small molecules will aid biological proof-of-concept studies which may lead to the development of novel therapeutic agents. Structure-based design efforts have focused on reducing the size and charge of Src SH2 ligands while increasing their ability to penetrate cells and reach the intracellular Src SH2 domain target. In this report we describe the synthesis, binding affinity, and Src SH2 cocrystal structure of a small, novel, nonpeptide, urea-containing SH2 domain ligand.

About this Structure

1SKJ is a Single protein structure of sequence from Rous sarcoma virus. Full crystallographic information is available from OCA.

Reference

Design, synthesis, and cocrystal structure of a nonpeptide Src SH2 domain ligand., Plummer MS, Holland DR, Shahripour A, Lunney EA, Fergus JH, Marks JS, McConnell P, Mueller WT, Sawyer TK, J Med Chem. 1997 Nov 7;40(23):3719-25. PMID:9371236

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