9pj1: Difference between revisions

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'''Unreleased structure'''


The entry 9pj1 is ON HOLD  until 2027-07-11
==Crystal structure of a synthetic Fab (4R) in complex with the ternary assembly of FKBP12, Rapamycin, and the FRB domain of mTOR==
 
<StructureSection load='9pj1' size='340' side='right'caption='[[9pj1]], [[Resolution|resolution]] 2.05&Aring;' scene=''>
Authors: O''Leary, K.M., Slezak, T., Kossiakoff, A.A.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9pj1]] is a 4 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=9PJ1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9PJ1 FirstGlance]. <br>
Description: Crystal structure of a synthetic Fab (4R) in complex with the ternary assembly of FKBP12, Rapamycin, and the FRB domain of mTOR
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.05&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=RAP:RAPAMYCIN+IMMUNOSUPPRESSANT+DRUG'>RAP</scene></td></tr>
[[Category: Kossiakoff, A.A]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9pj1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9pj1 OCA], [https://pdbe.org/9pj1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9pj1 RCSB], [https://www.ebi.ac.uk/pdbsum/9pj1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9pj1 ProSAT]</span></td></tr>
[[Category: Slezak, T]]
</table>
[[Category: O''Leary, K.M]]
== Function ==
[https://www.uniprot.org/uniprot/FKB1A_HUMAN FKB1A_HUMAN] Keeps in an inactive conformation TGFBR1, the TGF-beta type I serine/threonine kinase receptor, preventing TGF-beta receptor activation in absence of ligand. Recruites SMAD7 to ACVR1B which prevents the association of SMAD2 and SMAD3 with the activin receptor complex, thereby blocking the activin signal. May modulate the RYR1 calcium channel activity. PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides.<ref>PMID:9233797</ref> <ref>PMID:16720724</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Kossiakoff AA]]
[[Category: O'Leary KM]]
[[Category: Slezak T]]

Latest revision as of 07:12, 17 June 2026

Crystal structure of a synthetic Fab (4R) in complex with the ternary assembly of FKBP12, Rapamycin, and the FRB domain of mTOR

9pj1, resolution 2.05Å

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