2ye6
From Proteopedia
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==HSP90 inhibitors and drugs from fragment and virtual screening==  | ==HSP90 inhibitors and drugs from fragment and virtual screening==  | ||
| - | <StructureSection load='2ye6' size='340' side='right' caption='[[2ye6]], [[Resolution|resolution]] 2.56Å' scene=''>  | + | <StructureSection load='2ye6' size='340' side='right'caption='[[2ye6]], [[Resolution|resolution]] 2.56Å' scene=''>  | 
== Structural highlights ==  | == Structural highlights ==  | ||
| - | <table><tr><td colspan='2'>[[2ye6]] is a 1 chain structure with sequence from [  | + | <table><tr><td colspan='2'>[[2ye6]] 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=2YE6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2YE6 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">X-ray diffraction, [[Resolution|Resolution]] 2.56Å</td></tr>  | 
| - | <tr id='  | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=2AE:2-AMINO-BENZAMIDE'>2AE</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=2ye6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ye6 OCA], [https://pdbe.org/2ye6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2ye6 RCSB], [https://www.ebi.ac.uk/pdbsum/2ye6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2ye6 ProSAT]</span></td></tr>  | 
</table>  | </table>  | ||
== Function ==  | == Function ==  | ||
| - | [  | + | [https://www.uniprot.org/uniprot/HS90A_HUMAN HS90A_HUMAN] Molecular chaperone that promotes the maturation, structural maintenance and proper regulation of specific target proteins involved for instance in cell cycle control and signal transduction. Undergoes a functional cycle that is linked to its ATPase activity. This cycle probably induces conformational changes in the client proteins, thereby causing their activation. Interacts dynamically with various co-chaperones that modulate its substrate recognition, ATPase cycle and chaperone function.<ref>PMID:15937123</ref> <ref>PMID:11274138</ref>   | 
==See Also==  | ==See Also==  | ||
| - | *[[Heat Shock   | + | *[[Heat Shock Protein structures|Heat Shock Protein structures]]  | 
== References ==  | == References ==  | ||
<references/>  | <references/>  | ||
__TOC__  | __TOC__  | ||
</StructureSection>  | </StructureSection>  | ||
| - | [[Category:   | + | [[Category: Homo sapiens]]  | 
| - | [[Category:   | + | [[Category: Large Structures]]  | 
| - | [[Category:   | + | [[Category: Baker LM]]  | 
| - | [[Category:   | + | [[Category: Hubbard RE]]  | 
| - | [[Category:   | + | [[Category: Roughley SD]]  | 
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Current revision
HSP90 inhibitors and drugs from fragment and virtual screening
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