9bd8: Difference between revisions

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'''Unreleased structure'''


The entry 9bd8 is ON HOLD until Paper Publication
==ApoB 100 beta barrel bound to LDLR beta propeller==
 
<StructureSection load='9bd8' size='340' side='right'caption='[[9bd8]], [[Resolution|resolution]] 4.80&Aring;' scene=''>
Authors:  
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9bd8]] is a 2 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=9BD8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9BD8 FirstGlance]. <br>
Description:  
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 4.8&#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=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</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=9bd8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9bd8 OCA], [https://pdbe.org/9bd8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9bd8 RCSB], [https://www.ebi.ac.uk/pdbsum/9bd8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9bd8 ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/APOB_HUMAN APOB_HUMAN] Homozygous familial hypercholesterolemia. The disease is caused by variants affecting the gene represented in this entry. Most cases of FHBL1 result from nonsense mutations in the APOB gene that lead to a premature stop codon, which generate prematurely truncated apo B protein products (PubMed:21981844).<ref>PMID:21981844</ref>  The disease is caused by variants affecting the gene represented in this entry. Defects in APOB associated with defects in other genes (polygenic) can contribute to hypocholesterolemia.
== Function ==
[https://www.uniprot.org/uniprot/APOB_HUMAN APOB_HUMAN] Apolipoprotein B is a major protein constituent of chylomicrons (apo B-48), LDL (apo B-100) and VLDL (apo B-100). Apo B-100 functions as a recognition signal for the cellular binding and internalization of LDL particles by the apoB/E receptor.
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Dearborn AD]]
[[Category: Graziano G]]
[[Category: Kumar A]]
[[Category: Lei H]]
[[Category: Marcotrigiano J]]
[[Category: Neufeld EB]]
[[Category: Reimund M]]
[[Category: Remaley AT]]

Latest revision as of 09:30, 25 December 2024

ApoB 100 beta barrel bound to LDLR beta propeller

9bd8, resolution 4.80Å

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