3lpb: Difference between revisions
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{{STRUCTURE_3lpb| PDB=3lpb | SCENE= }} | |||
===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 | <!-- | ||
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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
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
- ↑ 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
Page seeded by OCA on Wed Apr 28 10:45:42 2010
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- Homo sapiens
- Non-specific protein-tyrosine kinase
- Furet, P.
- Gerspacher, M.
- Kroemer, M.
- Pissot-Soldermann, C.
- Tavares, G A.
- Atp site kinase inhibitor
- Atp-binding
- Chromosomal rearrangement
- Disease mutation
- Kinase
- Membrane
- Novartis product nvp-blu040
- Nucleotide-binding
- Phosphoprotein
- Polymorphism
- Proto-oncogene
- Sh2 domain
- Small molecule inhibitor
- Transferase
- Tyrosine-protein kinase