1ol1
From Proteopedia
(Difference between revisions)
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==About this Structure== | ==About this Structure== | ||
- | 1OL1 is a | + | 1OL1 is a 6 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=1OL1 OCA]. |
==Reference== | ==Reference== | ||
- | + | <ref group="xtra">PMID:14656438</ref><references group="xtra"/> | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Non-specific serine/threonine protein kinase]] | [[Category: Non-specific serine/threonine protein kinase]] | ||
- | [[Category: Protein complex]] | ||
[[Category: Andrews, M.]] | [[Category: Andrews, M.]] | ||
[[Category: Cowan, A.]] | [[Category: Cowan, A.]] | ||
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[[Category: Transfera serine/threonine-protein kinase]] | [[Category: Transfera serine/threonine-protein kinase]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 18:46:01 2009'' |
Revision as of 16:46, 16 February 2009
CYCLIN A BINDING GROOVE INHIBITOR H-CIT-CIT-LEU-ILE-(P-F-PHE)-NH2
Template:ABSTRACT PUBMED 14656438
About this Structure
1OL1 is a 6 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Kontopidis G, Andrews MJ, McInnes C, Cowan A, Powers H, Innes L, Plater A, Griffiths G, Paterson D, Zheleva DI, Lane DP, Green S, Walkinshaw MD, Fischer PM. Insights into cyclin groove recognition: complex crystal structures and inhibitor design through ligand exchange. Structure. 2003 Dec;11(12):1537-46. PMID:14656438
Page seeded by OCA on Mon Feb 16 18:46:01 2009
Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Andrews, M. | Cowan, A. | Fischer, P. | Green, S. | Griffiths, G. | Innes, L. | Kontopidis, G. | Lane, D. | Mcinnes, C. | Paterson, D. | Plater, A. | Powers, H. | Walkinshaw, M. | Zheleva, D. | Atp-binding | Cell cycle | Cell division | Cyclin some | Drug design | Inhibitor | Ligand exchange | Mitosis | Peptidomimetic | Phosphorylation | Transfera serine/threonine-protein kinase