1urw: Difference between revisions
New page: left|200px<br /> <applet load="1urw" size="450" color="white" frame="true" align="right" spinBox="true" caption="1urw, resolution 1.6Å" /> '''CDK2 IN COMPLEX WITH... |
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==About this Structure== | ==About this Structure== | ||
1URW is a [[http://en.wikipedia.org/wiki/Single_protein Single protein]] structure of sequence from [[http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]] with ACE and I1P as [[http://en.wikipedia.org/wiki/ligands ligands]]. Active as [[http://en.wikipedia.org/wiki/ ]], with EC number [[http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.37 2.7.1.37]]. Full crystallographic information is available from [[http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1URW OCA]]. | 1URW is a [[http://en.wikipedia.org/wiki/Single_protein Single protein]] structure of sequence from [[http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]] with ACE and I1P as [[http://en.wikipedia.org/wiki/ligands ligands]]. Active as [[http://en.wikipedia.org/wiki/Transferred_entry:_2.7.11.1 Transferred entry: 2.7.11.1]], with EC number [[http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.37 2.7.1.37]]. Structure known Active Site: AC2. Full crystallographic information is available from [[http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1URW OCA]]. | ||
==Reference== | ==Reference== | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Transferred entry: 2.7.11.1]] | |||
[[Category: Breed, J.]] | [[Category: Breed, J.]] | ||
[[Category: Byth, K.F.]] | [[Category: Byth, K.F.]] | ||
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[[Category: transferase]] | [[Category: transferase]] | ||
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Revision as of 14:19, 30 October 2007
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CDK2 IN COMPLEX WITH AN IMIDAZO[1,2-B]PYRIDAZINE
OverviewOverview
Modification of imidazo[1,2-a]pyridine CDK inhibitors lead to, identification of less lipophilic imidazo[1,2-b]pyridazine series of CDK, inhibitors. Although several equivalent compounds from these two series, have similar structure and show similar CDK activity, the SAR of the two, series differs significantly. Protein inhibitor structure determination, has confirmed differences in binding mode and given some understanding of, these differences in SAR. Potent and selective imidazo[1,2-b]pyridazine, inhibitors of CDK2 have been identified, which show >1 microM plasma, levels following a 2mg/kg oral dose to mice.
About this StructureAbout this Structure
1URW is a [Single protein] structure of sequence from [Homo sapiens] with ACE and I1P as [ligands]. Active as [Transferred entry: 2.7.11.1], with EC number [2.7.1.37]. Structure known Active Site: AC2. Full crystallographic information is available from [OCA].
ReferenceReference
Imidazo[1,2-b]pyridazines: a potent and selective class of cyclin-dependent kinase inhibitors., Byth KF, Cooper N, Culshaw JD, Heaton DW, Oakes SE, Minshull CA, Norman RA, Pauptit RA, Tucker JA, Breed J, Pannifer A, Rowsell S, Stanway JJ, Valentine AL, Thomas AP, Bioorg Med Chem Lett. 2004 May 3;14(9):2249-52. PMID:15081018
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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCA- Pages with broken file links
- Homo sapiens
- Single protein
- Transferred entry: 2.7.11.1
- Breed, J.
- Byth, K.F.
- Cooper, N.
- Culshaw, J.D.
- Heaton, D.W.
- Minshull, C.A.
- Norman, R.A.
- Oakes, S.E.
- Pannifer, A.
- Pauptit, R.A.
- Rowsell, S.
- Stanway, J.J.
- Thomas, A.P.
- Valentine, A.L.
- Yucker, J.A.
- ACE
- I1P
- Mitosis
- Serine/threonine-protein kinase
- Transferase