3j7y
From Proteopedia
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==Structure of the large ribosomal subunit from human mitochondria== | ==Structure of the large ribosomal subunit from human mitochondria== | ||
- | < | + | <SX load='3j7y' size='340' side='right' viewer='molstar' caption='[[3j7y]], [[Resolution|resolution]] 3.40Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[3j7y]] is a | + | <table><tr><td colspan='2'>[[3j7y]] is a 10 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=3J7Y OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3J7Y 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">Electron Microscopy, [[Resolution|Resolution]] 3.4Å</td></tr> |
- | <tr id=' | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AMP:ADENOSINE+MONOPHOSPHATE'>AMP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3j7y FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3j7y OCA], [https://pdbe.org/3j7y PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3j7y RCSB], [https://www.ebi.ac.uk/pdbsum/3j7y PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3j7y ProSAT]</span></td></tr> |
</table> | </table> | ||
- | == Disease == | ||
- | [[http://www.uniprot.org/uniprot/RM03_HUMAN RM03_HUMAN]] Combined oxidative phosphorylation defect type 9. The disease is caused by mutations affecting the gene represented in this entry. [[http://www.uniprot.org/uniprot/RM44_HUMAN RM44_HUMAN]] Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency. The disease is caused by mutations affecting the gene represented in this entry. | ||
== Function == | == Function == | ||
- | [ | + | [https://www.uniprot.org/uniprot/RM02_HUMAN RM02_HUMAN] |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
+ | <div class="pdbe-citations 3j7y" style="background-color:#fffaf0;"></div> | ||
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+ | ==See Also== | ||
+ | *[[Transfer RNA (tRNA)|Transfer RNA (tRNA)]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
- | </ | + | </SX> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Amunts | + | [[Category: Large Structures]] |
- | [[Category: Bai | + | [[Category: Amunts A]] |
- | [[Category: Brown | + | [[Category: Bai XC]] |
- | [[Category: Edwards | + | [[Category: Brown A]] |
- | [[Category: Murshudov | + | [[Category: Edwards PC]] |
- | [[Category: Ramakrishnan | + | [[Category: Murshudov G]] |
- | [[Category: Scheres | + | [[Category: Ramakrishnan V]] |
- | [[Category: Sugimoto | + | [[Category: Scheres SHW]] |
- | + | [[Category: Sugimoto Y]] | |
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Current revision
Structure of the large ribosomal subunit from human mitochondria
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Categories: Homo sapiens | Large Structures | Amunts A | Bai XC | Brown A | Edwards PC | Murshudov G | Ramakrishnan V | Scheres SHW | Sugimoto Y