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3rcd
From Proteopedia
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| - | + | [[Image:3rcd.jpg|left|200px]] | |
| - | The | + | <!-- |
| + | The line below this paragraph, containing "STRUCTURE_3rcd", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3rcd| PDB=3rcd | SCENE= }} | ||
| - | + | ===HER2 Kinase Domain Complexed with TAK-285=== | |
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| + | <!-- | ||
| + | The line below this paragraph, {{ABSTRACT_PUBMED_22003817}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 22003817 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_22003817}} | ||
| + | |||
| + | ==About this Structure== | ||
| + | [[3rcd]] is a 4 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=3RCD OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:022003817</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Receptor protein-tyrosine kinase]] | ||
| + | [[Category: Aertgeerts, K.]] | ||
| + | [[Category: Skene, R.]] | ||
| + | [[Category: Sogabe, S.]] | ||
| + | [[Category: Anti-oncogene]] | ||
| + | [[Category: Atp-binding]] | ||
| + | [[Category: Cell cycle]] | ||
| + | [[Category: Disease]] | ||
| + | [[Category: Glycoprotein]] | ||
| + | [[Category: Kinase domain]] | ||
| + | [[Category: Membrane]] | ||
| + | [[Category: Mutation]] | ||
| + | [[Category: Nucleotide-binding]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Receptor]] | ||
| + | [[Category: Secreted]] | ||
| + | [[Category: Transferase]] | ||
| + | [[Category: Transferase-transferase inhibitor complex]] | ||
| + | [[Category: Tyrosine kinase inhibitor]] | ||
| + | [[Category: Tyrosine-protein kinase]] | ||
Revision as of 19:04, 23 November 2011
HER2 Kinase Domain Complexed with TAK-285
Template:ABSTRACT PUBMED 22003817
About this Structure
3rcd is a 4 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Ishikawa T, Seto M, Banno H, Kawakita Y, Oorui M, Taniguchi T, Ohta Y, Tamura T, Nakayama A, Miki H, Kamiguchi H, Tanaka T, Habuka N, Sogabe S, Yano J, Aertgeerts K, Kamiyama K. Design and Synthesis of Novel Human Epidermal Growth Factor Receptor 2 (HER2)/Epidermal Growth Factor Receptor (EGFR) Dual Inhibitors Bearing a Pyrrolo[3,2-d]pyrimidine Scaffold. J Med Chem. 2011 Nov 4. PMID:22003817 doi:10.1021/jm2008634
Categories: Homo sapiens | Receptor protein-tyrosine kinase | Aertgeerts, K. | Skene, R. | Sogabe, S. | Anti-oncogene | Atp-binding | Cell cycle | Disease | Glycoprotein | Kinase domain | Membrane | Mutation | Nucleotide-binding | Phosphoprotein | Receptor | Secreted | Transferase | Transferase-transferase inhibitor complex | Tyrosine kinase inhibitor | Tyrosine-protein kinase
