3tcz: Difference between revisions

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[[Image:3tcz.jpg|left|200px]]


{{STRUCTURE_3tcz| PDB=3tcz | SCENE= }}  
==Human Pin1 bound to cis peptidomimetic inhibitor==
<StructureSection load='3tcz' size='340' side='right'caption='[[3tcz]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
== Structural highlights ==
<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>
</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>
<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>
<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>
</table>
== Function ==
[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>


===Human Pin1 bound to cis peptidomimetic inhibitor===
==See Also==
 
*[[Peptidyl-prolyl cis-trans isomerase 3D structures|Peptidyl-prolyl cis-trans isomerase 3D structures]]
{{ABSTRACT_PUBMED_22670809}}
== References ==
 
<references/>
==About this Structure==
__TOC__
[[3tcz]] 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=3TCZ OCA].
</StructureSection>
 
==Reference==
<ref group="xtra">PMID:022670809</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Peptidylprolyl isomerase]]
[[Category: Large Structures]]
[[Category: Zhang, M.]]
[[Category: Zhang M]]
[[Category: Zhang, Y.]]
[[Category: Zhang Y]]
[[Category: Isomerase-inhibitor complex]]
[[Category: Peptidyl-prolyl isomerase]]
[[Category: Ppiase domain]]
[[Category: Ww domain]]

Latest revision as of 10:07, 1 March 2024

Human Pin1 bound to cis peptidomimetic inhibitor

3tcz, resolution 2.10Å

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