3ug2
From Proteopedia
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- | + | [[Image:3ug2.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3ug2", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
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+ | {{STRUCTURE_3ug2| PDB=3ug2 | SCENE= }} | ||
- | + | ===Crystal structure of the mutated EGFR kinase domain (G719S/T790M) in complex with gefitinib=== | |
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+ | <!-- | ||
+ | The line below this paragraph, {{ABSTRACT_PUBMED_22349823}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 22349823 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_22349823}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | [[3ug2]] 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=3UG2 OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:022349823</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Receptor protein-tyrosine kinase]] | ||
+ | [[Category: Handa, N.]] | ||
+ | [[Category: Kukimoto-Niino, M.]] | ||
+ | [[Category: Parker, L J.]] | ||
+ | [[Category: Shirouzu, M.]] | ||
+ | [[Category: Yokoyama, S.]] | ||
+ | [[Category: Yoshikawa, S.]] | ||
+ | [[Category: Atp binding]] | ||
+ | [[Category: Cell cycle]] | ||
+ | [[Category: Disease mutation]] | ||
+ | [[Category: Drug resistance]] | ||
+ | [[Category: Kinase]] | ||
+ | [[Category: Phosphorylation]] | ||
+ | [[Category: Receptor]] | ||
+ | [[Category: Transferase-transferase inhibitor complex]] | ||
+ | [[Category: Transmembrane]] | ||
+ | [[Category: Tyrosine-protein kinase]] |
Revision as of 05:45, 8 March 2012
Crystal structure of the mutated EGFR kinase domain (G719S/T790M) in complex with gefitinib
Template:ABSTRACT PUBMED 22349823
About this Structure
3ug2 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Yoshikawa S, Kukimoto-Niino M, Parker L, Handa N, Terada T, Fujimoto T, Terazawa Y, Wakiyama M, Sato M, Sano S, Kobayashi T, Tanaka T, Chen L, Liu ZJ, Wang BC, Shirouzu M, Kawa S, Semba K, Yamamoto T, Yokoyama S. Structural basis for the altered drug sensitivities of non-small cell lung cancer-associated mutants of human epidermal growth factor receptor. Oncogene. 2012 Feb 20. doi: 10.1038/onc.2012.21. PMID:22349823 doi:10.1038/onc.2012.21
Categories: Homo sapiens | Receptor protein-tyrosine kinase | Handa, N. | Kukimoto-Niino, M. | Parker, L J. | Shirouzu, M. | Yokoyama, S. | Yoshikawa, S. | Atp binding | Cell cycle | Disease mutation | Drug resistance | Kinase | Phosphorylation | Receptor | Transferase-transferase inhibitor complex | Transmembrane | Tyrosine-protein kinase