2ms4: Difference between revisions
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==Cyclophilin a complexed with a fragment of crk-ii== | ==Cyclophilin a complexed with a fragment of crk-ii== | ||
<StructureSection load='2ms4' size='340' side='right'caption='[[2ms4 | <StructureSection load='2ms4' size='340' side='right'caption='[[2ms4]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2ms4]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[2ms4]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MS4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2MS4 FirstGlance]. <br> | ||
</td></tr> | </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=2ms4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ms4 OCA], [https://pdbe.org/2ms4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ms4 RCSB], [https://www.ebi.ac.uk/pdbsum/2ms4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ms4 ProSAT]</span></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=2ms4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ms4 OCA], [https://pdbe.org/2ms4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ms4 RCSB], [https://www.ebi.ac.uk/pdbsum/2ms4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ms4 ProSAT]</span></td></tr> | |||
</table> | </table> | ||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/PPIA_HUMAN PPIA_HUMAN] PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. | |||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Jankowski W]] | |||
[[Category: Jankowski | [[Category: Kalodimos C]] | ||
[[Category: Kalodimos | [[Category: Rossi P]] | ||
[[Category: Rossi | [[Category: Saleh T]] | ||
[[Category: Saleh | |||
Revision as of 11:05, 8 March 2023
Cyclophilin a complexed with a fragment of crk-iiCyclophilin a complexed with a fragment of crk-ii
Structural highlights
FunctionPPIA_HUMAN PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. Publication Abstract from PubMedCyclophilin A (CypA) is overexpressed in a number of human cancer types, but the mechanisms by which the protein promotes oncogenic properties of cells are not understood. Here we demonstrate that CypA binds the CrkII adaptor protein and prevents it from switching to the inhibited state. CrkII influences cell motility and invasion by mediating signaling through its SH2 and SH3 domains. CrkII Tyr221 phosphorylation by the Abl or EGFR kinases induces an inhibited state of CrkII by means of an intramolecular SH2-pTyr221 interaction, causing signaling interruption. We show that the CrkII phosphorylation site constitutes a binding site for CypA. Recruitment of CypA sterically restricts the accessibility of Tyr221 to kinases, thereby suppressing CrkII phosphorylation and promoting the active state. Structural, biophysical and in vivo data show that CypA augments CrkII-mediated signaling. A strong stimulation of cell migration is observed in cancer cells wherein both CypA and CrkII are greatly upregulated. Cyclophilin A promotes cell migration via the Abl-Crk signaling pathway.,Saleh T, Jankowski W, Sriram G, Rossi P, Shah S, Lee KB, Cruz LA, Rodriguez AJ, Birge RB, Kalodimos CG Nat Chem Biol. 2015 Dec 14. doi: 10.1038/nchembio.1981. PMID:26656091[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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