5vx3: Difference between revisions
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==Bcl-xL in complex with Bim-h3Pc-RT== | ==Bcl-xL in complex with Bim-h3Pc-RT== | ||
<StructureSection load='5vx3' size='340' side='right'caption='[[5vx3]], [[Resolution|resolution]] 1. | <StructureSection load='5vx3' size='340' side='right'caption='[[5vx3]], [[Resolution|resolution]] 1.95Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[5vx3]] is a 8 chain structure with sequence from [ | <table><tr><td colspan='2'>[[5vx3]] is a 8 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=5VX3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5VX3 FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.945Å</td></tr> | ||
<tr id=' | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=9R1:(2~{S})-2-azanyloctanedioic+acid'>9R1</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</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=5vx3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5vx3 OCA], [https://pdbe.org/5vx3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5vx3 RCSB], [https://www.ebi.ac.uk/pdbsum/5vx3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5vx3 ProSAT]</span></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/B2CL1_HUMAN B2CL1_HUMAN] Potent inhibitor of cell death. Inhibits activation of caspases (By similarity). Appears to regulate cell death by blocking the voltage-dependent anion channel (VDAC) by binding to it and preventing the release of the caspase activator, CYC1, from the mitochondrial membrane. Also acts as a regulator of G2 checkpoint and progression to cytokinesis during mitosis.<ref>PMID:19917720</ref> <ref>PMID:21840391</ref> Isoform Bcl-X(S) promotes apoptosis.<ref>PMID:19917720</ref> <ref>PMID:21840391</ref> | ||
<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: Brouwer | [[Category: Brouwer JM]] | ||
[[Category: Colman | [[Category: Colman PM]] | ||
[[Category: Cowan | [[Category: Cowan AD]] | ||
[[Category: Czabotar | [[Category: Czabotar PE]] | ||