3tdb

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[[Image:3tdb.png|left|200px]]
 
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{{STRUCTURE_3tdb| PDB=3tdb | SCENE= }}
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==Human Pin1 bound to trans peptidomimetic inhibitor==
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<StructureSection load='3tdb' size='340' side='right'caption='[[3tdb]], [[Resolution|resolution]] 2.27&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[3tdb]] 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=3TDB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3TDB 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]] 2.267&#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=3TB:N-[(1E,2R)-1-[(2R)-2-{[(2S)-1-AMINO-5-CARBAMIMIDAMIDO-1-OXOPENTAN-2-YL]CARBAMOYL}CYCLOPENTYLIDENE]-3-(PHOSPHONOOXY)PROPAN-2-YL]-L-PHENYLALANINAMIDE'>3TB</scene>, <scene name='pdbligand=PE4:2-{2-[2-(2-{2-[2-(2-ETHOXY-ETHOXY)-ETHOXY]-ETHOXY}-ETHOXY)-ETHOXY]-ETHOXY}-ETHANOL'>PE4</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=3tdb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3tdb OCA], [https://pdbe.org/3tdb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3tdb RCSB], [https://www.ebi.ac.uk/pdbsum/3tdb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3tdb 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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===Human Pin1 bound to trans peptidomimetic inhibitor===
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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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{{ABSTRACT_PUBMED_22670809}}
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== References ==
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<references/>
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==About this Structure==
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__TOC__
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[[3tdb]] 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=3TDB OCA].
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</StructureSection>
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==Reference==
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<ref group="xtra">PMID:022670809</ref><references group="xtra"/>
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Peptidylprolyl isomerase]]
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[[Category: Large Structures]]
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[[Category: Zhang, M.]]
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[[Category: Zhang M]]
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[[Category: Zhang, Y.]]
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[[Category: Zhang Y]]
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[[Category: Isomerase-inhibitor complex]]
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[[Category: Peptidyl-prolyl isomerase]]
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[[Category: Ppiase domain]]
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[[Category: Ww domain]]
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Current revision

Human Pin1 bound to trans peptidomimetic inhibitor

PDB ID 3tdb

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