9e9r
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 9e9r is ON HOLD Authors: Berndsen, Z.T., Cassidy, C.K. Description: The Structure of ApoB100 from Human Low-Density Lipoprotein [[Category: Unrelea...) |
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| - | '''Unreleased structure''' | ||
| - | The | + | ==The Structure of ApoB100 from Human Low-Density Lipoprotein== |
| - | + | <StructureSection load='9e9r' size='340' side='right'caption='[[9e9r]], [[Resolution|resolution]] 9.00Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[9e9r]] is a 1 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=9E9R OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9E9R FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 9Å</td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9e9r FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9e9r OCA], [https://pdbe.org/9e9r PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9e9r RCSB], [https://www.ebi.ac.uk/pdbsum/9e9r PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9e9r ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| - | [[Category: Berndsen | + | == 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: Berndsen ZT]] | ||
| + | [[Category: Cassidy CK]] | ||
Current revision
The Structure of ApoB100 from Human Low-Density Lipoprotein
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