1wbt: Difference between revisions
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[[Image:1wbt.png|left|200px]] | [[Image:1wbt.png|left|200px]] | ||
{{STRUCTURE_1wbt| PDB=1wbt | SCENE= }} | {{STRUCTURE_1wbt| PDB=1wbt | SCENE= }} | ||
===IDENTIFICATION OF NOVEL P38 ALPHA MAP KINASE INHIBITORS USING FRAGMENT-BASED LEAD GENERATION.=== | ===IDENTIFICATION OF NOVEL P38 ALPHA MAP KINASE INHIBITORS USING FRAGMENT-BASED LEAD GENERATION.=== | ||
{{ABSTRACT_PUBMED_15658855}} | {{ABSTRACT_PUBMED_15658855}} | ||
==About this Structure== | ==About this Structure== | ||
[[1wbt]] is a 1 chain structure of [[Mitogen-activated protein kinase]] with 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=1WBT OCA]. | |||
==See Also== | |||
*[[Mitogen-activated protein kinase|Mitogen-activated protein kinase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:015658855</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Non-specific serine/threonine protein kinase]] | [[Category: Non-specific serine/threonine protein kinase]] | ||
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[[Category: Tickle, J.]] | [[Category: Tickle, J.]] | ||
[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: Inhibitor structure]] | [[Category: Inhibitor structure]] | ||
[[Category: Nuclear protein]] | [[Category: Nuclear protein]] | ||
Line 38: | Line 28: | ||
[[Category: Serine/threonine-protein kinase]] | [[Category: Serine/threonine-protein kinase]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
Revision as of 15:06, 27 July 2012
IDENTIFICATION OF NOVEL P38 ALPHA MAP KINASE INHIBITORS USING FRAGMENT-BASED LEAD GENERATION.IDENTIFICATION OF NOVEL P38 ALPHA MAP KINASE INHIBITORS USING FRAGMENT-BASED LEAD GENERATION.
Template:ABSTRACT PUBMED 15658855
About this StructureAbout this Structure
1wbt is a 1 chain structure of Mitogen-activated protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See AlsoSee Also
ReferenceReference
- ↑ Gill AL, Frederickson M, Cleasby A, Woodhead SJ, Carr MG, Woodhead AJ, Walker MT, Congreve MS, Devine LA, Tisi D, O'Reilly M, Seavers LC, Davis DJ, Curry J, Anthony R, Padova A, Murray CW, Carr RA, Jhoti H. Identification of novel p38alpha MAP kinase inhibitors using fragment-based lead generation. J Med Chem. 2005 Jan 27;48(2):414-26. PMID:15658855 doi:10.1021/jm049575n