1g3n

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[[Image:1g3n.jpg|left|200px]]
[[Image:1g3n.jpg|left|200px]]
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{{Structure
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|PDB= 1g3n |SIZE=350|CAPTION= <scene name='initialview01'>1g3n</scene>, resolution 2.9&Aring;
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The line below this paragraph, containing "STRUCTURE_1g3n", creates the "Structure Box" on the page.
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|SITE=
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Non-specific_serine/threonine_protein_kinase Non-specific serine/threonine protein kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.1 2.7.11.1] </span>
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|GENE= CYCLIN-DEPENDENT KINASE 6 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), P18(INK4C) ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), K-CYCLIN (VIRAL CYCLIND HOMOLOG) ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=37296 Human herpesvirus 8])
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|DOMAIN=
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{{STRUCTURE_1g3n| PDB=1g3n | SCENE= }}
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|RELATEDENTRY=[[1bi7|1BI7]], [[1bi8|1BI8]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1g3n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1g3n OCA], [http://www.ebi.ac.uk/pdbsum/1g3n PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1g3n RCSB]</span>
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'''STRUCTURE OF A P18(INK4C)-CDK6-K-CYCLIN TERNARY COMPLEX'''
'''STRUCTURE OF A P18(INK4C)-CDK6-K-CYCLIN TERNARY COMPLEX'''
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[[Category: Pavletich, N P.]]
[[Category: Pavletich, N P.]]
[[Category: Tong, L.]]
[[Category: Tong, L.]]
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[[Category: cyclin-dependent kinase]]
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[[Category: Cyclin-dependent kinase]]
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[[Category: ink4 inhibitor]]
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[[Category: Ink4 inhibitor]]
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[[Category: viral cyclin]]
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[[Category: Viral cyclin]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 17:05:48 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:35:55 2008''
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Revision as of 14:05, 2 May 2008

Template:STRUCTURE 1g3n

STRUCTURE OF A P18(INK4C)-CDK6-K-CYCLIN TERNARY COMPLEX


Overview

The cyclin-dependent kinases 4 and 6 (Cdk4/6) that drive progression through the G(1) phase of the cell cycle play a central role in the control of cell proliferation, and CDK deregulation is a frequent event in cancer. Cdk4/6 are regulated by the D-type cyclins, which bind to CDKs and activate the kinase, and by the INK4 family of inhibitors. INK4 proteins can bind both monomeric CDK, preventing its association with a cyclin, and also the CDK-cyclin complex, forming an inactive ternary complex. In vivo, binary INK4-Cdk4/6 complexes are more abundant than ternary INK4-Cdk4/6-cyclinD complexes, and it has been suggested that INK4 binding may lead to the eventual dissociation of the cyclin. Here we present the 2.9-A crystal structure of the inactive ternary complex between Cdk6, the INK4 inhibitor p18(INK4c), and a D-type viral cyclin. The structure reveals that p18(INK4c) inhibits the CDK-cyclin complex by distorting the ATP binding site and misaligning catalytic residues. p18(INK4c) also distorts the cyclin-binding site, with the cyclin remaining bound at an interface that is substantially reduced in size. These observations support the model that INK4 binding weakens the cyclin's affinity for the CDK. This structure also provides insights into the specificity of the D-type cyclins for Cdk4/6.

About this Structure

1G3N is a Protein complex structure of sequences from Homo sapiens and Human herpesvirus 8. Full crystallographic information is available from OCA.

Reference

Structural basis of inhibition of CDK-cyclin complexes by INK4 inhibitors., Jeffrey PD, Tong L, Pavletich NP, Genes Dev. 2000 Dec 15;14(24):3115-25. PMID:11124804 Page seeded by OCA on Fri May 2 17:05:48 2008

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