2w06
From Proteopedia
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===STRUCTURE OF CDK2 IN COMPLEX WITH AN IMIDAZOLYL PYRIMIDINE, COMPOUND 5C=== | ===STRUCTURE OF CDK2 IN COMPLEX WITH AN IMIDAZOLYL PYRIMIDINE, COMPOUND 5C=== | ||
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+ | The line below this paragraph, {{ABSTRACT_PUBMED_18815031}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 18815031 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_18815031}} | ||
==About this Structure== | ==About this Structure== | ||
2W06 is a [[Single protein]] 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=2W06 OCA]. | 2W06 is a [[Single protein]] 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=2W06 OCA]. | ||
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+ | ==Reference== | ||
+ | Imidazoles: SAR and development of a potent class of cyclin-dependent kinase inhibitors., Anderson M, Andrews DM, Barker AJ, Brassington CA, Breed J, Byth KF, Culshaw JD, Finlay MR, Fisher E, McMiken HH, Green CP, Heaton DW, Nash IA, Newcombe NJ, Oakes SE, Pauptit RA, Roberts A, Stanway JJ, Thomas AP, Tucker JA, Walker M, Weir HM, Bioorg Med Chem Lett. 2008 Sep 10. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18815031 18815031] | ||
[[Category: Cyclin-dependent kinase]] | [[Category: Cyclin-dependent kinase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Transferase]] | [[Category: Transferase]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 29 09:48:38 2008'' |
Revision as of 07:48, 29 October 2008
STRUCTURE OF CDK2 IN COMPLEX WITH AN IMIDAZOLYL PYRIMIDINE, COMPOUND 5C
Template:ABSTRACT PUBMED 18815031
About this Structure
2W06 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Imidazoles: SAR and development of a potent class of cyclin-dependent kinase inhibitors., Anderson M, Andrews DM, Barker AJ, Brassington CA, Breed J, Byth KF, Culshaw JD, Finlay MR, Fisher E, McMiken HH, Green CP, Heaton DW, Nash IA, Newcombe NJ, Oakes SE, Pauptit RA, Roberts A, Stanway JJ, Thomas AP, Tucker JA, Walker M, Weir HM, Bioorg Med Chem Lett. 2008 Sep 10. PMID:18815031
Page seeded by OCA on Wed Oct 29 09:48:38 2008
Categories: Cyclin-dependent kinase | Homo sapiens | Single protein | Anderson, M. | Andrews, D M. | Barker, A J. | Brassington, C A. | Byth, K F. | Culshaw, J D. | Finlay, M R.V. | Fisher, E. | Green, C P. | Heaton, D W. | Mcmiken, H H.J. | Nash, I A. | Newcombe, N J. | Oakes, S E. | Roberts, A. | Stanway, J J. | Thomas, A P. | Tucker, J A. | Weir, H M. | Atp-binding | Cell cycle | Cell division | Kinase | Mitosis | Nucleotide-binding | Phosphoprotein | Phosphorylation | Polymorphism | Serine/threonine-protein kinase | Transferase