1h1r: Difference between revisions

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==About this Structure==
==About this Structure==
1H1R is a [[Protein complex]] structure of sequences 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=1H1R OCA].  
1H1R is a 4 chains structure of sequences 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=1H1R OCA].  


==Reference==
==Reference==
Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor., Davies TG, Bentley J, Arris CE, Boyle FT, Curtin NJ, Endicott JA, Gibson AE, Golding BT, Griffin RJ, Hardcastle IR, Jewsbury P, Johnson LN, Mesguiche V, Newell DR, Noble ME, Tucker JA, Wang L, Whitfield HJ, Nat Struct Biol. 2002 Oct;9(10):745-9. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/12244298 12244298]
<ref group="xtra">PMID:12244298</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Davies, T G.]]
[[Category: Davies, T G.]]
[[Category: Endicott, J A.]]
[[Category: Endicott, J A.]]
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[[Category: Transferase]]
[[Category: Transferase]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 17:51:54 2009''

Revision as of 18:51, 16 February 2009

File:1h1r.png

Template:STRUCTURE 1h1r

STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU6086STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU6086

Template:ABSTRACT PUBMED 12244298

About this StructureAbout this Structure

1H1R is a 4 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

[xtra 1]

  1. Davies TG, Bentley J, Arris CE, Boyle FT, Curtin NJ, Endicott JA, Gibson AE, Golding BT, Griffin RJ, Hardcastle IR, Jewsbury P, Johnson LN, Mesguiche V, Newell DR, Noble ME, Tucker JA, Wang L, Whitfield HJ. Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor. Nat Struct Biol. 2002 Oct;9(10):745-9. PMID:12244298 doi:http://dx.doi.org/10.1038/nsb842

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