7tfm
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Atomic Structure of the Leishmania spp. Hsp100 N-Domain== | |
| + | <StructureSection load='7tfm' size='340' side='right'caption='[[7tfm]], [[Resolution|resolution]] 1.05Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[7tfm]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Leishmania_mexicana_MHOM/GT/2001/U1103 Leishmania mexicana MHOM/GT/2001/U1103]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7TFM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7TFM FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.055Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</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=7tfm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7tfm OCA], [https://pdbe.org/7tfm PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7tfm RCSB], [https://www.ebi.ac.uk/pdbsum/7tfm PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7tfm ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/E9ALU6_LEIMU E9ALU6_LEIMU] | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Hsp100 is an ATP-dependent unfoldase that promotes protein disaggregation or facilitates the unfolding of aggregation-prone polypeptides marked for degradation. Recently, new Hsp100 functions are emerging. In Plasmodium, an Hsp100 drives malaria protein export, presenting a novel drug target. Whether Hsp100 has a similar function in other protists is unknown. We present the 1.06-A resolution crystal structure of the Hsp100 N-domain from Leishmania spp., the causative agent of leishmaniasis in humans. Our structure reveals a network of methionines and aromatic amino acids that define the putative substrate-binding site and likely evolved to protect Hsp100 from oxidative damage in host immune cells. | ||
| - | + | Atomic Structure of the Leishmania spp. Hsp100 N-Domain.,Mercado JM, Lee S, Chang C, Sung N, Soong L, Catic A, Tsai FTF Proteins. 2022 Feb 4. doi: 10.1002/prot.26310. PMID:35122310<ref>PMID:35122310</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | [[Category: | + | </div> |
| + | <div class="pdbe-citations 7tfm" style="background-color:#fffaf0;"></div> | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Heat Shock Protein structures|Heat Shock Protein structures]] | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Leishmania mexicana MHOM/GT/2001/U1103]] | ||
| + | [[Category: Catic A]] | ||
| + | [[Category: Chang C]] | ||
| + | [[Category: Lee S]] | ||
| + | [[Category: Mercado JM]] | ||
| + | [[Category: Soong L]] | ||
| + | [[Category: Sung N]] | ||
| + | [[Category: Tsai FTF]] | ||
Current revision
Atomic Structure of the Leishmania spp. Hsp100 N-Domain
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