3efw

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'''Unreleased structure'''
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{{Seed}}
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[[Image:3efw.jpg|left|200px]]
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The entry 3efw is ON HOLD until Paper Publication
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{{STRUCTURE_3efw| PDB=3efw | SCENE= }}
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Authors: Bellon, S.F., Cee, V., Hughes, P., Geuns-Meyer, S., Whittington, D.
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===Structure of AuroraA with pyridyl-pyrimidine urea inhibitor===
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Description: Structure of AuroraA with pyridyl-pyrimidine urea inhibitor
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 15 14:05:22 2008''
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{{ABSTRACT_PUBMED_19062275}}
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==About this Structure==
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3EFW is a 2 chains structure of sequences 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=3EFW OCA].
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==Reference==
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Pyridyl-pyrimidine benzimidazole derivatives as potent, selective, and orally bioavailable inhibitors of Tie-2 kinase., Cee VJ, Cheng AC, Romero K, Bellon S, Mohr C, Whittington DA, Bak A, Bready J, Caenepeel S, Coxon A, Deak HL, Fretland J, Gu Y, Hodous BL, Huang X, Kim JL, Lin J, Long AM, Nguyen H, Olivieri PR, Patel VF, Wang L, Zhou Y, Hughes P, Geuns-Meyer S, Bioorg Med Chem Lett. 2008 Nov 20. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/19062275 19062275]
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[[Category: Homo sapiens]]
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[[Category: Non-specific serine/threonine protein kinase]]
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[[Category: Bellon, S F.]]
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[[Category: Cee, V.]]
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[[Category: Geuns-Meyer, S.]]
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[[Category: Hughes, P.]]
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[[Category: Whittington, D.]]
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[[Category: Atp-binding]]
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[[Category: Auroraa]]
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[[Category: Cell cycle]]
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[[Category: Kinase]]
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[[Category: Nucleotide-binding]]
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[[Category: Phosphoprotein]]
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[[Category: Polymorphism]]
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[[Category: Serine/threonine-protein kinase]]
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[[Category: Stk6_human]]
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[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 24 11:31:51 2008''

Revision as of 09:31, 24 December 2008

Image:3efw.jpg

Template:STRUCTURE 3efw

Structure of AuroraA with pyridyl-pyrimidine urea inhibitor

Template:ABSTRACT PUBMED 19062275

About this Structure

3EFW is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Pyridyl-pyrimidine benzimidazole derivatives as potent, selective, and orally bioavailable inhibitors of Tie-2 kinase., Cee VJ, Cheng AC, Romero K, Bellon S, Mohr C, Whittington DA, Bak A, Bready J, Caenepeel S, Coxon A, Deak HL, Fretland J, Gu Y, Hodous BL, Huang X, Kim JL, Lin J, Long AM, Nguyen H, Olivieri PR, Patel VF, Wang L, Zhou Y, Hughes P, Geuns-Meyer S, Bioorg Med Chem Lett. 2008 Nov 20. PMID:19062275

Page seeded by OCA on Wed Dec 24 11:31:51 2008

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