3emg

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'''Unreleased structure'''
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{{Seed}}
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[[Image:3emg.jpg|left|200px]]
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The entry 3emg is ON HOLD
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{{STRUCTURE_3emg| PDB=3emg | SCENE= }}
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Authors: Ter Haar, E.
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===Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)===
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Description: Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 15 14:05:58 2008''
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{{ABSTRACT_PUBMED_18938080}}
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==About this Structure==
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3EMG is a 1 chain structure of 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=3EMG OCA].
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==Reference==
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Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)., Farmer LJ, Bemis G, Britt SD, Cochran J, Connors M, Harrington EM, Hoock T, Markland W, Nanthakumar S, Taslimi P, Ter Haar E, Wang J, Zhaveri D, Salituro FG, Bioorg Med Chem Lett. 2008 Dec 1;18(23):6231-5. Epub 2008 Oct 7. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18938080 18938080]
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[[Category: Homo sapiens]]
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[[Category: Non-specific protein-tyrosine kinase]]
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[[Category: Pdbx_ordinal=, <PDBx:audit_author.]]
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[[Category: Alternative splicing]]
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[[Category: Atp-binding]]
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[[Category: Host-virus interaction]]
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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: Sh2 domain]]
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[[Category: Syk]]
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[[Category: Transferase]]
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[[Category: Tyrosine-protein kinase]]
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[[Category: Ubl conjugation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Dec 5 09:40:51 2008''

Revision as of 07:40, 5 December 2008

Template:STRUCTURE 3emg

Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)

Template:ABSTRACT PUBMED 18938080

About this Structure

3EMG is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Discovery and SAR of novel 4-thiazolyl-2-phenylaminopyrimidines as potent inhibitors of spleen tyrosine kinase (SYK)., Farmer LJ, Bemis G, Britt SD, Cochran J, Connors M, Harrington EM, Hoock T, Markland W, Nanthakumar S, Taslimi P, Ter Haar E, Wang J, Zhaveri D, Salituro FG, Bioorg Med Chem Lett. 2008 Dec 1;18(23):6231-5. Epub 2008 Oct 7. PMID:18938080[[Category: Pdbx_ordinal=, <PDBx:audit_author.]]

Page seeded by OCA on Fri Dec 5 09:40:51 2008

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