3bv3: Difference between revisions
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[[Image:3bv3.png|left|200px]] | [[Image:3bv3.png|left|200px]] | ||
{{STRUCTURE_3bv3| PDB=3bv3 | SCENE= }} | {{STRUCTURE_3bv3| PDB=3bv3 | SCENE= }} | ||
===Morpholino pyrrolotriazine P38 Alpha Map Kinase inhibitor compound 2=== | ===Morpholino pyrrolotriazine P38 Alpha Map Kinase inhibitor compound 2=== | ||
{{ABSTRACT_PUBMED_18364256}} | {{ABSTRACT_PUBMED_18364256}} | ||
==About this Structure== | ==About this Structure== | ||
[[3bv3]] 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=3BV3 OCA]. | |||
==See Also== | |||
*[[Mitogen-activated protein kinase|Mitogen-activated protein kinase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:018364256</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Mitogen-activated protein kinase]] | [[Category: Mitogen-activated protein kinase]] | ||
[[Category: Sack, J S.]] | [[Category: Sack, J S.]] | ||
[[Category: Atp-binding]] | [[Category: Atp-binding]] | ||
[[Category: Kinase]] | [[Category: Kinase]] | ||
[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
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[[Category: Serine/threonine-protein kinase]] | [[Category: Serine/threonine-protein kinase]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
Revision as of 19:37, 26 July 2012
Morpholino pyrrolotriazine P38 Alpha Map Kinase inhibitor compound 2
Template:ABSTRACT PUBMED 18364256
About this Structure
3bv3 is a 1 chain structure of Mitogen-activated protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Wrobleski ST, Lin S, Hynes J Jr, Wu H, Pitt S, Shen DR, Zhang R, Gillooly KM, Shuster DJ, McIntyre KW, Doweyko AM, Kish KF, Tredup JA, Duke GJ, Sack JS, McKinnon M, Dodd J, Barrish JC, Schieven GL, Leftheris K. Synthesis and SAR of new pyrrolo[2,1-f][1,2,4]triazines as potent p38 alpha MAP kinase inhibitors. Bioorg Med Chem Lett. 2008 Apr 15;18(8):2739-44. Epub 2008 Mar 4. PMID:18364256 doi:10.1016/j.bmcl.2008.02.067