View source for 6cyi


==Grp94 N-domain bound to NEOCA==
<StructureSection load='6cyi' size='340' side='right'caption='[[6cyi]], [[Resolution|resolution]] 1.76&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6cyi]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Canis_lupus_familiaris Canis lupus familiaris]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6CYI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6CYI 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]] 1.7565825&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=N5O:5-N-(2-HYDROXYL)ETHYL+CARBOXYAMIDO+ADENOSINE'>N5O</scene>, <scene name='pdbligand=PG4:TETRAETHYLENE+GLYCOL'>PG4</scene>, <scene name='pdbligand=PGE:TRIETHYLENE+GLYCOL'>PGE</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=6cyi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6cyi OCA], [https://pdbe.org/6cyi PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6cyi RCSB], [https://www.ebi.ac.uk/pdbsum/6cyi PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6cyi ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/ENPL_CANLF ENPL_CANLF] Molecular chaperone that functions in the processing and transport of secreted proteins. When associated with CNPY3, required for proper folding of Toll-like receptors. Functions in endoplasmic reticulum associated degradation (ERAD). Has ATPase activity (By similarity).
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== Publication Abstract from PubMed ==
The hsp90 chaperones govern the function of essential client proteins critical to normal cell function as well as cancer initiation and progression. Hsp90 activity is driven by ATP, which binds to the N-terminal domain (NTD) and induces large conformational changes that are required for client maturation. Inhibitors targeting the ATP binding pocket of the NTD have anticancer effects, but most bind with similar affinity to cytosolic Hsp90alpha and beta, endoplasmic reticulum Grp94, and mitochondrial Trap1, the four cellular hsp90 paralogs. Paralog-specific inhibitors may lead to drugs with fewer side effects. The ATP binding pockets of the four paralogs are flanked by three side pockets, termed Sites 1, 2, and 3, which differ between the paralogs in their accessibility to inhibitors. Previous insights into the principles governing access to Sites 1 and 2 have resulted in the development of paralog-selective inhibitors targeting these sites, but the rules for selective targeting of Site 3 are less clear. Previous work identified 5'N-ethylcarboxamido adenosine (NECA) as a Grp94-selective ligand. Here, we use NECA and its derivatives to probe the properties of Site 3. We found that derivatives that lengthen the 5' moiety of NECA improve selectivity for Grp94 over Hsp90alpha. Crystal structures reveal that the derivatives extend further into Site 3 of Grp94 compared to their parent compound and that selectivity is due to paralog-specific differences in ligand pose and ligand-induced conformational strain in the protein. These studies provide a structural basis for Grp94-selective inhibition using Site 3.

NECA derivatives exploit the paralog-specific properties of the Site 3 side pocket of Grp94, the ER Hsp90.,Huck JD, Que NLS, Immormino RM, Shrestha L, Taldone T, Chiosis G, Gewirth DT J Biol Chem. 2019 Sep 9. pii: RA119.009960. doi: 10.1074/jbc.RA119.009960. PMID:31501246<ref>PMID:31501246</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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<div class="pdbe-citations 6cyi" style="background-color:#fffaf0;"></div>

==See Also==
*[[Heat Shock Protein structures|Heat Shock Protein structures]]
== References ==
<references/>
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</StructureSection>
[[Category: Canis lupus familiaris]]
[[Category: Large Structures]]
[[Category: Aw WJ]]
[[Category: Gewirth DT]]
[[Category: Huck JD]]