2yej: Difference between revisions

New page: '''Unreleased structure''' The entry 2yej is ON HOLD Authors: Roughley, S.D., Hubbard, R.E., BAKER, L.M. Description: HSP90 inhibitors and drugs from fragment and virtual screening
 
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'''Unreleased structure'''


The entry 2yej is ON HOLD
==HSP90 inhibitors and drugs from fragment and virtual screening==
<StructureSection load='2yej' size='340' side='right'caption='[[2yej]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[2yej]] 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=2YEJ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2YEJ 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]] 2.2&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=XQK:METHYL+5-ISOXAZOL-5-YL-3-METHYL-1H-PYRAZOLE-4-CARBOXYLATE'>XQK</scene>, <scene name='pdbligand=ZZ3:4-METHYL-6-(METHYLSULFANYL)-1,3,5-TRIAZIN-2-AMINE'>ZZ3</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=2yej FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2yej OCA], [https://pdbe.org/2yej PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2yej RCSB], [https://www.ebi.ac.uk/pdbsum/2yej PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2yej ProSAT]</span></td></tr>
</table>
== 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>


Authors: Roughley, S.D., Hubbard, R.E., BAKER, L.M.
==See Also==
 
*[[Heat Shock Protein structures|Heat Shock Protein structures]]
Description: HSP90 inhibitors and drugs from fragment and virtual screening
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Baker LM]]
[[Category: Hubbard RE]]
[[Category: Roughley SD]]

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