6tpg

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m (Protected "6tpg" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6tpg is ON HOLD
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==Crystal structure of the Orexin-2 receptor in complex with EMPA at 2.74 A resolution==
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<StructureSection load='6tpg' size='340' side='right'caption='[[6tpg]], [[Resolution|resolution]] 2.74&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6tpg]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6TPG OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6TPG FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=7MA:N-ethyl-2-[(6-methoxypyridin-3-yl)-(2-methylphenyl)sulfonyl-amino]-N-(pyridin-3-ylmethyl)ethanamide'>7MA</scene>, <scene name='pdbligand=OLA:OLEIC+ACID'>OLA</scene>, <scene name='pdbligand=PG4:TETRAETHYLENE+GLYCOL'>PG4</scene></td></tr>
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<tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=YCM:S-(2-AMINO-2-OXOETHYL)-L-CYSTEINE'>YCM</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6tpg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6tpg OCA], [http://pdbe.org/6tpg PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6tpg RCSB], [http://www.ebi.ac.uk/pdbsum/6tpg PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6tpg ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/OX2R_HUMAN OX2R_HUMAN]] Nonselective, high-affinity receptor for both orexin-A and orexin-B neuropeptides.
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The orexin system, which consists of the two G protein-coupled receptors OX1 and OX2, activated by the neuropeptides OX-A and OX-B, is firmly established as a key regulator of behavioural arousal, sleep and wakefulness, and has been an area of intense research effort over the past two decades. X-ray structures of the receptors in complex with ten new antagonist ligands from diverse chemotypes are presented, which complement the existing structural information for the system and highlight the critical importance of lipophilic hotspots and water molecules for these peptidergic GPCR targets. Learnings from the structural information regarding the utility of pharmacophore models and how selectivity between OX1 and OX2 can be achieved are discussed.
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Authors:
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Comparison of orexin 1 and orexin 2 ligand binding modes using X-ray crystallography and computational analysis.,Rappas M, Ali A, Bennett KA, Brown JD, Bucknell SJ, Congreve M, Cooke RM, Cseke G, de Graaf C, Dore AS, Errey JC, Jazayeri A, Marshall FH, Mason JS, Mould R, Patel JC, Tehan B, Weir M, Christopher JA J Med Chem. 2019 Dec 20. doi: 10.1021/acs.jmedchem.9b01787. PMID:31860301<ref>PMID:31860301</ref>
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Description:
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 6tpg" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Ali, A]]
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[[Category: Bennett, K A]]
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[[Category: Brown, J D]]
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[[Category: Bucknell, S J]]
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[[Category: Christopher, J A]]
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[[Category: Congreve, M]]
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[[Category: Cooke, R M]]
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[[Category: Cseke, G]]
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[[Category: Dore, A S]]
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[[Category: Errey, J C]]
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[[Category: Graaf, C de]]
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[[Category: Jazayeri, A]]
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[[Category: Marshall, F H]]
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[[Category: Mason, J S]]
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[[Category: Mould, R]]
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[[Category: Patel, J C]]
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[[Category: Rappas, M]]
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[[Category: Tehan, B G]]
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[[Category: Weir, M]]
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[[Category: Gpcr]]
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[[Category: Membrane protein]]

Revision as of 08:27, 1 January 2020

Crystal structure of the Orexin-2 receptor in complex with EMPA at 2.74 A resolution

PDB ID 6tpg

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