3oz1
From Proteopedia
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| - | + | ==cIAP1-BIR3 domain in complex with the Smac-mimetic compound Smac066== | |
| - | ===cIAP1-BIR3 domain in complex with the Smac-mimetic compound Smac066 | + | <StructureSection load='3oz1' size='340' side='right' caption='[[3oz1]], [[Resolution|resolution]] 3.00Å' scene=''> |
| - | + | == Structural highlights == | |
| + | <table><tr><td colspan='2'>[[3oz1]] is a 4 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=3OZ1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3OZ1 FirstGlance]. <br> | ||
| + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BMB:(3S,6S,7R,9AS)-7-[2-(BENZYLAMINO)ETHYL]-N-(DIPHENYLMETHYL)-6-{[(2S)-2-(METHYLAMINO)BUTANOYL]AMINO}-5-OXOOCTAHYDRO-1H-PYRROLO[1,2-A]AZEPINE-3-CARBOXAMIDE'>BMB</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> | ||
| + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3mup|3mup]]</td></tr> | ||
| + | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">BIRC2, API1, IAP2, MIHB, RNF48 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr> | ||
| + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3oz1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3oz1 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=3oz1 RCSB], [http://www.ebi.ac.uk/pdbsum/3oz1 PDBsum]</span></td></tr> | ||
| + | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Inhibitor of apoptosis proteins (IAPs) are negative regulators of apoptosis. Since IAPs are overexpressed in many tumors, where they confer chemoresistance, small molecules inactivating IAPs have been proposed as anticancer agents. Accordingly, a number of IAP-binding pro-apoptotic compounds that mimic the sequence corresponding to the N-terminal tetrapeptide of Smac/DIABLO, the natural endogenous IAPs inhibitor, have been developed. Here we report the crystal structures of the BIR3 domain of cIAP1 in complex with Smac037, a Smac-mimetic known to bind potently to the XIAP-BIR3 domain and to induce degradation of cIAP1, and in complex with the novel Smac-mimetic compound Smac066. Thermal stability and fluorescence polarization assays show the stabilizing effect and the high affinity of both Smac037 and Smac066 for cIAP1- and cIAP2-BIR3 domains. | ||
| - | + | Recognition of Smac-mimetic compounds by the BIR3 domain of cIAP1.,Cossu F, Malvezzi F, Canevari G, Mastrangelo E, Lecis D, Delia D, Seneci P, Scolastico C, Bolognesi M, Milani M Protein Sci. 2010 Oct 15. PMID:20954235<ref>PMID:20954235</ref> | |
| - | + | ||
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | + | </div> | |
| - | + | == References == | |
| - | == | + | <references/> |
| - | + | __TOC__ | |
| + | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Bolognesi, M | + | [[Category: Bolognesi, M]] |
| - | [[Category: Canevari, G | + | [[Category: Canevari, G]] |
| - | [[Category: Cossu, F | + | [[Category: Cossu, F]] |
| - | [[Category: Malvezzi, F | + | [[Category: Malvezzi, F]] |
| - | [[Category: Mastrangelo, E | + | [[Category: Mastrangelo, E]] |
| - | [[Category: Milani, M | + | [[Category: Milani, M]] |
[[Category: Apoptosis inhibitor]] | [[Category: Apoptosis inhibitor]] | ||
[[Category: Caspase]] | [[Category: Caspase]] | ||
[[Category: Zinc-finger]] | [[Category: Zinc-finger]] | ||
Revision as of 07:20, 19 December 2014
cIAP1-BIR3 domain in complex with the Smac-mimetic compound Smac066
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