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2vww
From Proteopedia
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[[Image:2vww.png|left|200px]] | [[Image:2vww.png|left|200px]] | ||
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{{STRUCTURE_2vww| PDB=2vww | SCENE= }} | {{STRUCTURE_2vww| PDB=2vww | SCENE= }} | ||
===EPHB4 KINASE DOMAIN INHIBITOR COMPLEX=== | ===EPHB4 KINASE DOMAIN INHIBITOR COMPLEX=== | ||
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{{ABSTRACT_PUBMED_18434142}} | {{ABSTRACT_PUBMED_18434142}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[2vww]] is a 1 chain structure of [[Ephrin receptor]] 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=2VWW OCA]. | |
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| + | ==See Also== | ||
| + | *[[Ephrin receptor|Ephrin receptor]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:018434142</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Receptor protein-tyrosine kinase]] | [[Category: Receptor protein-tyrosine kinase]] | ||
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[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
| - | [[Category: Polymorphism]] | ||
[[Category: Receptor]] | [[Category: Receptor]] | ||
[[Category: Receptor tyrosine kinase]] | [[Category: Receptor tyrosine kinase]] | ||
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[[Category: Tyrosine-protein kinase]] | [[Category: Tyrosine-protein kinase]] | ||
[[Category: Unphosphorylated]] | [[Category: Unphosphorylated]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 12:25:30 2009'' | ||
Revision as of 16:56, 26 July 2012
Contents |
EPHB4 KINASE DOMAIN INHIBITOR COMPLEX
Template:ABSTRACT PUBMED 18434142
About this Structure
2vww is a 1 chain structure of Ephrin receptor with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Bardelle C, Cross D, Davenport S, Kettle JG, Ko EJ, Leach AG, Mortlock A, Read J, Roberts NJ, Robins P, Williams EJ. Inhibitors of the tyrosine kinase EphB4. Part 1: Structure-based design and optimization of a series of 2,4-bis-anilinopyrimidines. Bioorg Med Chem Lett. 2008 May 1;18(9):2776-80. Epub 2008 Apr 10. PMID:18434142 doi:10.1016/j.bmcl.2008.04.015
Categories: Homo sapiens | Receptor protein-tyrosine kinase | Barratt, D. | Brassington, C A. | Green, I. | Kettle, J G. | Leach, A G. | Mccall, E J. | Read, J. | Valentine, A L. | Atp-binding | Glycoprotein | Kinase | Membrane | Mutant | Nucleotide-binding | Phosphoprotein | Receptor | Receptor tyrosine kinase | Transferase | Transmembrane | Tyrosine-protein kinase | Unphosphorylated
