2cjm
From Proteopedia
(New page: 200px<br /> <applet load="2cjm" size="450" color="white" frame="true" align="right" spinBox="true" caption="2cjm, resolution 2.30Å" /> '''MECHANISM OF CDK IN...) |
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==About this Structure== | ==About this Structure== | ||
| - | 2CJM is a [[http://en.wikipedia.org/wiki/Protein_complex Protein complex]] structure of sequences from [[http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]] with MG, PTR and ATP 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=2CJM OCA]]. | + | 2CJM is a [[http://en.wikipedia.org/wiki/Protein_complex Protein complex]] structure of sequences from [[http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]] with MG, PTR and ATP 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: AC1. Full crystallographic information is available from [[http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2CJM OCA]]. |
==Reference== | ==Reference== | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
| + | [[Category: Transferred entry: 2.7.11.1]] | ||
[[Category: Endicott, J.A.]] | [[Category: Endicott, J.A.]] | ||
[[Category: Johnson, T.]] | [[Category: Johnson, T.]] | ||
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[[Category: transferase]] | [[Category: transferase]] | ||
| - | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Oct 30 13:44:46 2007'' |
Revision as of 11:40, 30 October 2007
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MECHANISM OF CDK INHIBITION BY ACTIVE SITE PHOSPHORYLATION: CDK2 Y15P T160P IN COMPLEX WITH CYCLIN A STRUCTURE
Overview
Inhibition of cyclin-dependent kinase 1 (CDK1) activity by Tyr-15, phosphorylation directly regulates entry into mitosis and is an important, element in the control of the unperturbed cell cycle. Active site, phosphorylation of other members of the CDK family that regulate cell, cycle progression instates checkpoints that are fundamental to eukaryotic, cell cycle regulation. Kinetic and crystallographic analyses of, CDK2-cyclin A complexes reveal that this inhibitory mechanism operates, through steric blockade of peptide substrate binding and through the, creation of an environment that favors a non-productive conformation of, the terminal group of ATP. By contrast, tyrosine phosphorylation of CDK2, alters neither its Km for ATP nor its significant intrinsic ATPase, activity. ... [(full description)]
About this Structure
2CJM is a [Protein complex] structure of sequences from [Homo sapiens] with MG, PTR and ATP as [ligands]. Active as [Transferred entry: 2.7.11.1], with EC number [2.7.1.37]. Structure known Active Site: AC1. Full crystallographic information is available from [OCA].
Reference
How tyrosine 15 phosphorylation inhibits the activity of cyclin-dependent kinase 2-cyclin A., Welburn JP, Tucker JA, Johnson T, Lindert L, Morgan M, Willis A, Noble ME, Endicott JA, J Biol Chem. 2007 Feb 2;282(5):3173-81. Epub 2006 Nov 9. PMID:17095507
Page seeded by OCA on Tue Oct 30 13:44:46 2007
Categories: Homo sapiens | Protein complex | Transferred entry: 2.7.11.1 | Endicott, J.A. | Johnson, T. | Lindert, L. | Noble, M.E.M. | Tucker, J. | Welburn, J.P.I. | Willis, A. | ATP | MG | PTR | Atp-binding | Cell cycle | Cell division | Complex (transferase/cell division) | Cyclin | Cyclin-dependent kinase | Kinase | Mitosis | Nucleotide-binding | Phosphorylation | Polymorphism | Regulation | Serine/threonine-protein kinase | Transferase
