1g5s

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[[Image:1g5s.gif|left|200px]]
[[Image:1g5s.gif|left|200px]]
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{{Structure
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|PDB= 1g5s |SIZE=350|CAPTION= <scene name='initialview01'>1g5s</scene>, resolution 2.61&Aring;
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The line below this paragraph, containing "STRUCTURE_1g5s", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=I17:2-[TRANS-(4-AMINOCYCLOHEXYL)AMINO]-6-(BENZYL-AMINO)-9-CYCLOPENTYLPURINE'>I17</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|GENE= CDK2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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{{STRUCTURE_1g5s| PDB=1g5s | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1g5s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1g5s OCA], [http://www.ebi.ac.uk/pdbsum/1g5s PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1g5s RCSB]</span>
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'''CRYSTAL STRUCTURE OF HUMAN CYCLIN DEPENDENT KINASE 2 (CDK2) IN COMPLEX WITH THE INHIBITOR H717'''
'''CRYSTAL STRUCTURE OF HUMAN CYCLIN DEPENDENT KINASE 2 (CDK2) IN COMPLEX WITH THE INHIBITOR H717'''
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[[Category: Tsay, J T.]]
[[Category: Tsay, J T.]]
[[Category: Wright, P S.]]
[[Category: Wright, P S.]]
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[[Category: protein-inhibitor complex]]
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[[Category: Protein-inhibitor complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 17:10:19 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:37:10 2008''
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Revision as of 14:10, 2 May 2008

Template:STRUCTURE 1g5s

CRYSTAL STRUCTURE OF HUMAN CYCLIN DEPENDENT KINASE 2 (CDK2) IN COMPLEX WITH THE INHIBITOR H717


Overview

Cyclin-dependent kinases (CDKs) are regulatory proteins of the eukaryotic cell cycle. They act after association with different cyclins, the concentrations of which vary throughout the progression of the cell cycle. As central mediators of cell growth, CDKs are potential targets for inhibitory molecules that would allow disruption of the cell cycle in order to evoke an antiproliferative effect and may therefore be useful as cancer therapeutics. We synthesized several inhibitory 2,6,9-trisubstituted purine derivatives and solved the crystal structure of one of these compounds, H717, in complex with human CDK2 at 2.6 A resolution. The orientation of the C2-p-diaminocyclohexyl portion of the inhibitor is strikingly different from those of similar moieties in other related inhibitor complexes. The N9-cyclopentyl ring fully occupies a space in the enzyme which is otherwise empty, while the C6-N-aminobenzyl substituent points out of the ATP-binding site. The structure provides a basis for the further development of more potent inhibitory drugs.

About this Structure

1G5S is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Crystal structure of human cyclin-dependent kinase 2 in complex with the adenine-derived inhibitor H717., Dreyer MK, Borcherding DR, Dumont JA, Peet NP, Tsay JT, Wright PS, Bitonti AJ, Shen J, Kim SH, J Med Chem. 2001 Feb 15;44(4):524-30. PMID:11170642 Page seeded by OCA on Fri May 2 17:10:19 2008

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