3fdn
From Proteopedia
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| - | + | [[Image:3fdn.png|left|200px]] | |
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{{STRUCTURE_3fdn| PDB=3fdn | SCENE= }} | {{STRUCTURE_3fdn| PDB=3fdn | SCENE= }} | ||
===Structure-based drug design of novel Aurora kinase A inhibitors: Structure basis for potency and specificity=== | ===Structure-based drug design of novel Aurora kinase A inhibitors: Structure basis for potency and specificity=== | ||
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| - | (as it appears on PubMed at http://www.pubmed.gov), where 19140666 is the PubMed ID number. | ||
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{{ABSTRACT_PUBMED_19140666}} | {{ABSTRACT_PUBMED_19140666}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[3fdn]] 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=3FDN OCA]. | |
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:019140666</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Non-specific serine/threonine protein kinase]] | [[Category: Non-specific serine/threonine protein kinase]] | ||
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[[Category: Nucleotide-binding]] | [[Category: Nucleotide-binding]] | ||
[[Category: Phosphoprotein]] | [[Category: Phosphoprotein]] | ||
| - | [[Category: Polymorphism]] | ||
[[Category: Serine/threonine-protein kinase]] | [[Category: Serine/threonine-protein kinase]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
[[Category: Virtual screening]] | [[Category: Virtual screening]] | ||
[[Category: X-ray co-crystal analysis]] | [[Category: X-ray co-crystal analysis]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 16 08:58:03 2009'' | ||
Revision as of 11:14, 13 February 2013
Structure-based drug design of novel Aurora kinase A inhibitors: Structure basis for potency and specificity
Template:ABSTRACT PUBMED 19140666
About this Structure
3fdn is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Coumar MS, Leou JS, Shukla P, Wu JS, Dixit AK, Lin WH, Chang CY, Lien TW, Tan UK, Chen CH, Hsu JT, Chao YS, Wu SY, Hsieh HP. Structure-based drug design of novel Aurora kinase A inhibitors: structural basis for potency and specificity. J Med Chem. 2009 Feb 26;52(4):1050-62. PMID:19140666 doi:10.1021/jm801270e
Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Coumar, M S. | Hsieh, H P. | Leou, J S. | Shukla, P. | Wu, J S. | Wu, S Y. | Atp-binding | Aurora kinase inhibitor | Cell cycle | H-bonding. | Kinase | Nucleotide-binding | Phosphoprotein | Serine/threonine-protein kinase | Transferase | Virtual screening | X-ray co-crystal analysis
