3kai: Difference between revisions
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{{STRUCTURE_3kai| PDB=3kai | SCENE= }} | {{STRUCTURE_3kai| PDB=3kai | SCENE= }} | ||
===Structure-guided design of alpha-amino acid-derived Pin1 inhibitors=== | ===Structure-guided design of alpha-amino acid-derived Pin1 inhibitors=== | ||
{{ABSTRACT_PUBMED_19969456}} | |||
==Function== | |||
[[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> | |||
==About this Structure== | ==About this Structure== | ||
[[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: | <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]] | ||