1ol1
From Proteopedia
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{{STRUCTURE_1ol1| PDB=1ol1 | SCENE= }} | {{STRUCTURE_1ol1| PDB=1ol1 | SCENE= }} | ||
===CYCLIN A BINDING GROOVE INHIBITOR H-CIT-CIT-LEU-ILE-(P-F-PHE)-NH2=== | ===CYCLIN A BINDING GROOVE INHIBITOR H-CIT-CIT-LEU-ILE-(P-F-PHE)-NH2=== | ||
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{{ABSTRACT_PUBMED_14656438}} | {{ABSTRACT_PUBMED_14656438}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1ol1]] is a 6 chain structure of [[Cell Division Protein Kinase 2]] and [[Cyclin]] with 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=1OL1 OCA]. | |
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| + | ==See Also== | ||
| + | *[[Cell Division Protein Kinase 2|Cell Division Protein Kinase 2]] | ||
| + | *[[Cyclin|Cyclin]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:014656438</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Non-specific serine/threonine protein kinase]] | [[Category: Non-specific serine/threonine protein kinase]] | ||
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[[Category: Drug design]] | [[Category: Drug design]] | ||
[[Category: Inhibitor]] | [[Category: Inhibitor]] | ||
| + | [[Category: Kinase-cyclin complex]] | ||
[[Category: Ligand exchange]] | [[Category: Ligand exchange]] | ||
[[Category: Mitosis]] | [[Category: Mitosis]] | ||
[[Category: Peptidomimetic]] | [[Category: Peptidomimetic]] | ||
[[Category: Phosphorylation]] | [[Category: Phosphorylation]] | ||
| - | [[Category: | + | [[Category: Serine/threonine-protein kinase]] |
| - | [[Category: Transferase | + | [[Category: Transferase-transferase inhibitor complex]] |
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Revision as of 21:06, 25 July 2012
Contents |
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 chain structure of Cell Division Protein Kinase 2 and Cyclin with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
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
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 | Kinase-cyclin complex | Ligand exchange | Mitosis | Peptidomimetic | Phosphorylation | Serine/threonine-protein kinase | Transferase-transferase inhibitor complex
