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4xue

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(New page: '''Unreleased structure''' The entry 4xue is ON HOLD Authors: Allison, T., Wolkenberg, S., Sanders, J.M., Soisson, S.M. Description: Synthesis and evaluation of heterocyclic catechol m...)
Current revision (13:01, 1 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 4xue is ON HOLD
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==Synthesis and evaluation of heterocyclic catechol mimics as inhibitors of catechol-O-methyltransferase (COMT): Structure with Cmpd27b==
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<StructureSection load='4xue' size='340' side='right'caption='[[4xue]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4xue]] is a 2 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=4XUE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4XUE FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.3&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=43J:2-(BIPHENYL-3-YL)-5-HYDROXY-3-METHYLPYRIMIDIN-4(3H)-ONE'>43J</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4xue FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4xue OCA], [https://pdbe.org/4xue PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4xue RCSB], [https://www.ebi.ac.uk/pdbsum/4xue PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4xue ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/COMT_HUMAN COMT_HUMAN] Catalyzes the O-methylation, and thereby the inactivation, of catecholamine neurotransmitters and catechol hormones. Also shortens the biological half-lives of certain neuroactive drugs, like L-DOPA, alpha-methyl DOPA and isoproterenol.
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Authors: Allison, T., Wolkenberg, S., Sanders, J.M., Soisson, S.M.
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==See Also==
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*[[Catechol O-methyltransferase 3D structures|Catechol O-methyltransferase 3D structures]]
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Description: Synthesis and evaluation of heterocyclic catechol mimics as inhibitors of catechol-O-methyltransferase (COMT): Structure with Cmpd27b
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__TOC__
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[[Category: Unreleased Structures]]
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</StructureSection>
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[[Category: Allison, T]]
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[[Category: Homo sapiens]]
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[[Category: Sanders, J.M]]
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[[Category: Large Structures]]
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[[Category: Soisson, S.M]]
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[[Category: Allison T]]
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[[Category: Wolkenberg, S]]
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[[Category: Sanders JM]]
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[[Category: Soisson SM]]
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[[Category: Wolkenberg S]]

Current revision

Synthesis and evaluation of heterocyclic catechol mimics as inhibitors of catechol-O-methyltransferase (COMT): Structure with Cmpd27b

PDB ID 4xue

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