3et7
From Proteopedia
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| + | The line below this paragraph, containing "STRUCTURE_3et7", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3et7| PDB=3et7 | SCENE= }} | ||
| - | + | ===Crystal structure of PYK2 complexed with PF-2318841=== | |
| - | Description: Crystal structure of PYK2 complexed with PF-2318841 | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_18951788}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 18951788 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_18951788}} | ||
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| + | ==About this Structure== | ||
| + | 3ET7 is a 1 chain structure of 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=3ET7 OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:18951788</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Non-specific protein-tyrosine kinase]] | ||
| + | [[Category: Han, S.]] | ||
| + | [[Category: Alternative splicing]] | ||
| + | [[Category: Atp-binding]] | ||
| + | [[Category: Cell membrane]] | ||
| + | [[Category: Cytoplasm]] | ||
| + | [[Category: Kinase]] | ||
| + | [[Category: Membrane]] | ||
| + | [[Category: Nucleotide-binding]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Signaling protein]] | ||
| + | [[Category: Transferase]] | ||
| + | [[Category: Tyrosine-protein kinase]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Jun 25 09:17:49 2009'' | ||
Revision as of 06:17, 25 June 2009
Crystal structure of PYK2 complexed with PF-2318841
Template:ABSTRACT PUBMED 18951788
About this Structure
3ET7 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Walker DP, Bi FC, Kalgutkar AS, Bauman JN, Zhao SX, Soglia JR, Aspnes GE, Kung DW, Klug-McLeod J, Zawistoski MP, McGlynn MA, Oliver R, Dunn M, Li JC, Richter DT, Cooper BA, Kath JC, Hulford CA, Autry CL, Luzzio MJ, Ung EJ, Roberts WG, Bonnette PC, Buckbinder L, Mistry A, Griffor MC, Han S, Guzman-Perez A. Trifluoromethylpyrimidine-based inhibitors of proline-rich tyrosine kinase 2 (PYK2): structure-activity relationships and strategies for the elimination of reactive metabolite formation. Bioorg Med Chem Lett. 2008 Dec 1;18(23):6071-7. Epub 2008 Oct 11. PMID:18951788 doi:10.1016/j.bmcl.2008.10.030
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