3tcz

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'''Unreleased structure'''
 
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The entry 3tcz is ON HOLD
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==Human Pin1 bound to cis peptidomimetic inhibitor==
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<StructureSection load='3tcz' size='340' side='right'caption='[[3tcz]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[3tcz]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3TCZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3TCZ FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PE4:2-{2-[2-(2-{2-[2-(2-ETHOXY-ETHOXY)-ETHOXY]-ETHOXY}-ETHOXY)-ETHOXY]-ETHOXY}-ETHANOL'>PE4</scene>, <scene name='pdbligand=R2Z:N~2~-({(1R,2Z)-2-[(2R)-2-(FORMYLAMINO)-3-(PHOSPHONOOXY)PROPYLIDENE]CYCLOPENTYL}CARBONYL)-L-ARGININAMIDE'>R2Z</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3tcz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3tcz OCA], [https://pdbe.org/3tcz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3tcz RCSB], [https://www.ebi.ac.uk/pdbsum/3tcz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3tcz ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://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>
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Authors: Zhang, M., Zhang, Y.
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==See Also==
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*[[Peptidyl-prolyl cis-trans isomerase 3D structures|Peptidyl-prolyl cis-trans isomerase 3D structures]]
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Description: Human Pin1 bound to cis peptidomimetic inhibitor
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Zhang M]]
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[[Category: Zhang Y]]

Current revision

Human Pin1 bound to cis peptidomimetic inhibitor

PDB ID 3tcz

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