3lpb: Difference between revisions

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'''Unreleased structure'''
{{Seed}}
[[Image:3lpb.jpg|left|200px]]


The entry 3lpb is ON HOLD until Paper Publication
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{{STRUCTURE_3lpb|  PDB=3lpb  |  SCENE=  }}


Authors: Tavares, G.A., Pissot-Soldermann, C., Gerspacher, M., Furet, P., Kroemer, M.
===Crystal structure of Jak2 complexed with a potent 2,8-diaryl-quinoxaline inhibitor===


Description: Crystal structure of Jak2 complexed with a potent 2,8-diaryl-quinoxaline inhibitor


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 10 13:13:41 2010''
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{{ABSTRACT_PUBMED_20231096}}
 
==About this Structure==
3LPB is a 2 chains structure with sequences 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=3LPB OCA].
 
==Reference==
<ref group="xtra">PMID:20231096</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Non-specific protein-tyrosine kinase]]
[[Category: Furet, P.]]
[[Category: Gerspacher, M.]]
[[Category: Kroemer, M.]]
[[Category: Pissot-Soldermann, C.]]
[[Category: Tavares, G A.]]
[[Category: Atp site kinase inhibitor]]
[[Category: Atp-binding]]
[[Category: Chromosomal rearrangement]]
[[Category: Disease mutation]]
[[Category: Kinase]]
[[Category: Membrane]]
[[Category: Novartis product nvp-blu040]]
[[Category: Nucleotide-binding]]
[[Category: Phosphoprotein]]
[[Category: Polymorphism]]
[[Category: Proto-oncogene]]
[[Category: Sh2 domain]]
[[Category: Small molecule inhibitor]]
[[Category: Transferase]]
[[Category: Tyrosine-protein kinase]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Apr 28 10:45:42 2010''

Revision as of 10:45, 28 April 2010

File:3lpb.jpg

Template:STRUCTURE 3lpb

Crystal structure of Jak2 complexed with a potent 2,8-diaryl-quinoxaline inhibitorCrystal structure of Jak2 complexed with a potent 2,8-diaryl-quinoxaline inhibitor

Template:ABSTRACT PUBMED 20231096

About this StructureAbout this Structure

3LPB is a 2 chains structure with sequences from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

[xtra 1]

  1. Pissot-Soldermann C, Gerspacher M, Furet P, Gaul C, Holzer P, McCarthy C, Radimerski T, Regnier CH, Baffert F, Drueckes P, Tavares GA, Vangrevelinghe E, Blasco F, Ottaviani G, Ossola F, Scesa J, Reetz J. Discovery and SAR of potent, orally available 2,8-diaryl-quinoxalines as a new class of JAK2 inhibitors. Bioorg Med Chem Lett. 2010 Apr 15;20(8):2609-13. Epub 2010 Feb 19. PMID:20231096 doi:10.1016/j.bmcl.2010.02.056

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