3kai: Difference between revisions

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[[Image:3kai.png|left|200px]]
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{{STRUCTURE_3kai|  PDB=3kai  |  SCENE=  }}  
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===Structure-guided design of alpha-amino acid-derived Pin1 inhibitors===
===Structure-guided design of alpha-amino acid-derived Pin1 inhibitors===
{{ABSTRACT_PUBMED_19969456}}


 
==Function==
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[[http://www.uniprot.org/uniprot/PIN1_HUMAN PIN1_HUMAN]] Essential PPIase that regulates mitosis presumably by interacting with NIMA and attenuating its mitosis-promoting activity. Displays a preference for an acidic residue N-terminal to the isomerized proline bond. Catalyzes pSer/Thr-Pro cis/trans isomerizations. Down-regulates kinase activity of BTK. Can transactivate multiple oncogenes and induce centrosome amplification, chromosome instability and cell transformation. Required for the efficient dephosphorylation and recycling of RAF1 after mitogen activation.<ref>PMID:15664191</ref> <ref>PMID:16644721</ref> <ref>PMID:21497122</ref>
The line below this paragraph, {{ABSTRACT_PUBMED_19969456}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_19969456}}


==About this Structure==
==About this Structure==
3KAI is a 1 chain structure of 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=3KAI OCA].  
[[3kai]] is a 1 chain structure 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=3KAI OCA].  


==Reference==
==Reference==
<ref group="xtra">PMID:19969456</ref><references group="xtra"/>
<ref group="xtra">PMID:019969456</ref><references group="xtra"/><references/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Peptidylprolyl isomerase]]
[[Category: Peptidylprolyl isomerase]]
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[[Category: Sbdd]]
[[Category: Sbdd]]
[[Category: Small molecule]]
[[Category: Small molecule]]
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