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3txo
From Proteopedia
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| - | + | [[Image:3txo.jpg|left|200px]] | |
| - | The | + | <!-- |
| + | The line below this paragraph, containing "STRUCTURE_3txo", creates the "Structure Box" on the page. | ||
| + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
| + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
| + | or leave the SCENE parameter empty for the default display. | ||
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| + | {{STRUCTURE_3txo| PDB=3txo | SCENE= }} | ||
| - | + | ===PKC eta kinase in complex with a naphthyridine=== | |
| - | + | ||
| + | <!-- | ||
| + | The line below this paragraph, {{ABSTRACT_PUBMED_22078216}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 22078216 is the PubMed ID number. | ||
| + | --> | ||
| + | {{ABSTRACT_PUBMED_22078216}} | ||
| + | |||
| + | ==About this Structure== | ||
| + | [[3txo]] is a 1 chain structure 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=3TXO OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:022078216</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Protein kinase C]] | ||
| + | [[Category: Cowan-Jacob, S W.]] | ||
| + | [[Category: Rummel, G.]] | ||
| + | [[Category: Stark, W.]] | ||
| + | [[Category: Kinase]] | ||
| + | [[Category: Phosphotransferase]] | ||
| + | [[Category: Transferase-transferase inhibitor complex]] | ||
Revision as of 06:12, 30 November 2011
PKC eta kinase in complex with a naphthyridine
Template:ABSTRACT PUBMED 22078216
About this Structure
3txo is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- van Eis MJ, Evenou JP, Floersheim P, Gaul C, Cowan-Jacob SW, Monovich L, Rummel G, Schuler W, Stark W, Strauss A, Matt A, Vangrevelinghe E, Wagner J, Soldermann N. 2,6-Naphthyridines as potent and selective inhibitors of the novel protein kinase C isozymes. Bioorg Med Chem Lett. 2011 Dec 15;21(24):7367-72. Epub 2011 Oct 21. PMID:22078216 doi:10.1016/j.bmcl.2011.10.025
