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1qmz
From Proteopedia
(Difference between revisions)
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{{STRUCTURE_1qmz| PDB=1qmz | SCENE= }} | {{STRUCTURE_1qmz| PDB=1qmz | SCENE= }} | ||
===PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX=== | ===PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX=== | ||
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{{ABSTRACT_PUBMED_10559988}} | {{ABSTRACT_PUBMED_10559988}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1qmz]] 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=1QMZ OCA]. | |
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| + | ==See Also== | ||
| + | *[[Cell Division Protein Kinase 2|Cell Division Protein Kinase 2]] | ||
| + | *[[Cyclin|Cyclin]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:010559988</ref><ref group="xtra">PMID:011738041</ref><ref group="xtra">PMID:012502784</ref><ref group="xtra">PMID:012904290</ref><ref group="xtra">PMID:014960716</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Brown, N R.]] | [[Category: Brown, N R.]] | ||
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[[Category: Noble, M E.M.]] | [[Category: Noble, M E.M.]] | ||
[[Category: Cdk]] | [[Category: Cdk]] | ||
| + | [[Category: Cell cycle]] | ||
[[Category: Cyclin]] | [[Category: Cyclin]] | ||
[[Category: Phosphorylation]] | [[Category: Phosphorylation]] | ||
[[Category: Substrate complex]] | [[Category: Substrate complex]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 05:58:03 2009'' | ||
Revision as of 12:23, 27 July 2012
Contents |
PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX
Template:ABSTRACT PUBMED 10559988
About this Structure
1qmz 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 Also
Reference
- Brown NR, Noble ME, Endicott JA, Johnson LN. The structural basis for specificity of substrate and recruitment peptides for cyclin-dependent kinases. Nat Cell Biol. 1999 Nov;1(7):438-43. PMID:10559988 doi:10.1038/15674
- Bax B, Carter PS, Lewis C, Guy AR, Bridges A, Tanner R, Pettman G, Mannix C, Culbert AA, Brown MJ, Smith DG, Reith AD. The structure of phosphorylated GSK-3beta complexed with a peptide, FRATtide, that inhibits beta-catenin phosphorylation. Structure. 2001 Dec;9(12):1143-52. PMID:11738041
- Brinkworth RI, Breinl RA, Kobe B. Structural basis and prediction of substrate specificity in protein serine/threonine kinases. Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):74-9. Epub 2002 Dec 26. PMID:12502784 doi:10.1073/pnas.0134224100
- Pei Y, Shuman S. Characterization of the Schizosaccharomyces pombe Cdk9/Pch1 protein kinase: Spt5 phosphorylation, autophosphorylation, and mutational analysis. J Biol Chem. 2003 Oct 31;278(44):43346-56. Epub 2003 Aug 5. PMID:12904290 doi:http://dx.doi.org/10.1074/jbc.M307319200
- Iakoucheva LM, Radivojac P, Brown CJ, O'Connor TR, Sikes JG, Obradovic Z, Dunker AK. The importance of intrinsic disorder for protein phosphorylation. Nucleic Acids Res. 2004 Feb 11;32(3):1037-49. Print 2004. PMID:14960716 doi:10.1093/nar/gkh253
