1vjy

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[[Image:1vjy.gif|left|200px]]
[[Image:1vjy.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1vjy |SIZE=350|CAPTION= <scene name='initialview01'>1vjy</scene>, resolution 2.0&Aring;
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The line below this paragraph, containing "STRUCTURE_1vjy", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=460:2-[5-(6-METHYLPYRIDIN-2-YL)-2,3-DIHYDRO-1H-PYRAZOL-4-YL]-1,5-NAPHTHYRIDINE'>460</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Non-specific_serine/threonine_protein_kinase Non-specific serine/threonine protein kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.1 2.7.11.1] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1vjy| PDB=1vjy | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1vjy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1vjy OCA], [http://www.ebi.ac.uk/pdbsum/1vjy PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1vjy RCSB]</span>
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}}
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'''Crystal Structure of a Naphthyridine Inhibitor of Human TGF-beta Type I Receptor'''
'''Crystal Structure of a Naphthyridine Inhibitor of Human TGF-beta Type I Receptor'''
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[[Category: Wang, R.]]
[[Category: Wang, R.]]
[[Category: Woolven, J.]]
[[Category: Woolven, J.]]
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[[Category: inhibitor complex]]
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[[Category: Inhibitor complex]]
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[[Category: protein kinase]]
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[[Category: Protein kinase]]
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[[Category: transferase]]
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[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 12:37:10 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:25:29 2008''
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Revision as of 09:37, 3 May 2008

Image:1vjy.gif

Template:STRUCTURE 1vjy

Crystal Structure of a Naphthyridine Inhibitor of Human TGF-beta Type I Receptor


Overview

Optimization of the screening hit 1 led to the identification of novel 1,5-naphthyridine aminothiazole and pyrazole derivatives, which are potent and selective inhibitors of the transforming growth factor-beta type I receptor, ALK5. Compounds 15 and 19, which inhibited ALK5 autophosphorylation with IC50 = 6 and 4 nM, respectively, showed potent activities in both binding and cellular assays and exhibited selectivity over p38 mitogen-activated protein kinase. The X-ray crystal structure of 19 in complex with human ALK5 is described, confirming the binding mode proposed from docking studies.

About this Structure

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

Reference

Identification of 1,5-naphthyridine derivatives as a novel series of potent and selective TGF-beta type I receptor inhibitors., Gellibert F, Woolven J, Fouchet MH, Mathews N, Goodland H, Lovegrove V, Laroze A, Nguyen VL, Sautet S, Wang R, Janson C, Smith W, Krysa G, Boullay V, De Gouville AC, Huet S, Hartley D, J Med Chem. 2004 Aug 26;47(18):4494-506. PMID:15317461 Page seeded by OCA on Sat May 3 12:37:10 2008

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