1urc: Difference between revisions
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[[Image:1urc.png|left|200px]] | [[Image:1urc.png|left|200px]] | ||
{{STRUCTURE_1urc| PDB=1urc | SCENE= }} | {{STRUCTURE_1urc| PDB=1urc | SCENE= }} | ||
===CYCLIN A BINDING GROOVE INHIBITOR ACE-ARG-LYS-LEU-PHE-GLY=== | ===CYCLIN A BINDING GROOVE INHIBITOR ACE-ARG-LYS-LEU-PHE-GLY=== | ||
{{ABSTRACT_PUBMED_15455144}} | {{ABSTRACT_PUBMED_15455144}} | ||
==About this Structure== | ==About this Structure== | ||
[[1urc]] 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=1URC OCA]. | |||
==See Also== | |||
*[[Cell Division Protein Kinase 2|Cell Division Protein Kinase 2]] | |||
*[[Cyclin|Cyclin]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:015455144</ref><references group="xtra"/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Non-specific serine/threonine protein kinase]] | [[Category: Non-specific serine/threonine protein kinase]] | ||
| Line 43: | Line 35: | ||
[[Category: Drug design]] | [[Category: Drug design]] | ||
[[Category: Inhibitor]] | [[Category: Inhibitor]] | ||
[[Category: Kinase]] | |||
[[Category: Ligand exchange]] | [[Category: Ligand exchange]] | ||
[[Category: Peptidomimetic]] | [[Category: Peptidomimetic]] | ||
Revision as of 16:15, 27 July 2012
CYCLIN A BINDING GROOVE INHIBITOR ACE-ARG-LYS-LEU-PHE-GLYCYCLIN A BINDING GROOVE INHIBITOR ACE-ARG-LYS-LEU-PHE-GLY
Template:ABSTRACT PUBMED 15455144
About this StructureAbout this Structure
1urc 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 AlsoSee Also
ReferenceReference
- ↑ Andrews MJ, McInnes C, Kontopidis G, Innes L, Cowan A, Plater A, Fischer PM. Design, synthesis, biological activity and structural analysis of cyclic peptide inhibitors targeting the substrate recruitment site of cyclin-dependent kinase complexes. Org Biomol Chem. 2004 Oct 7;2(19):2735-41. Epub 2004 Sep 9. PMID:15455144 doi:10.1039/B409157D
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- 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.
- Cyclin some
- Drug design
- Inhibitor
- Kinase
- Ligand exchange
- Peptidomimetic