1oit
From Proteopedia
(Difference between revisions)
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{{STRUCTURE_1oit| PDB=1oit | SCENE= }} | {{STRUCTURE_1oit| PDB=1oit | SCENE= }} | ||
- | + | ===IMIDAZOPYRIDINES: A POTENT AND SELECTIVE CLASS OF CYCLIN-DEPENDENT KINASE INHIBITORS IDENTIFIED THROUGH STRUCTURE-BASED HYBRIDISATION=== | |
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- | + | The line below this paragraph, {{ABSTRACT_PUBMED_12941325}}, adds the Publication Abstract to the page | |
+ | (as it appears on PubMed at http://www.pubmed.gov), where 12941325 is the PubMed ID number. | ||
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==About this Structure== | ==About this Structure== | ||
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[[Category: Thomas, A P.]] | [[Category: Thomas, A P.]] | ||
[[Category: Protein kinase]] | [[Category: Protein kinase]] | ||
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+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 20:08:31 2008'' |
Revision as of 17:08, 28 July 2008
IMIDAZOPYRIDINES: A POTENT AND SELECTIVE CLASS OF CYCLIN-DEPENDENT KINASE INHIBITORS IDENTIFIED THROUGH STRUCTURE-BASED HYBRIDISATION
Template:ABSTRACT PUBMED 12941325
About this Structure
1OIT is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Imidazo[1,2-a]pyridines: a potent and selective class of cyclin-dependent kinase inhibitors identified through structure-based hybridisation., Anderson M, Beattie JF, Breault GA, Breed J, Byth KF, Culshaw JD, Ellston RP, Green S, Minshull CA, Norman RA, Pauptit RA, Stanway J, Thomas AP, Jewsbury PJ, Bioorg Med Chem Lett. 2003 Sep 15;13(18):3021-6. PMID:12941325
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