3oe5: Difference between revisions
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New page: '''Unreleased structure''' The entry 3oe5 is ON HOLD Authors: Rudolph, M.G. Description: RAT CATECHOL O-METHYLTRANSFERASE IN COMPLEX WITH A BISUBSTRATE INHIBITOR -HUMANIZED FORM ''Pag... |
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==Rat catechol O-methyltransferase in complex with a catechol-type, pyridylsulfanyl-containing inhibitor - humanized form== | |||
<StructureSection load='3oe5' size='340' side='right'caption='[[3oe5]], [[Resolution|resolution]] 1.52Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[3oe5]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3OE5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3OE5 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]] 1.52Å</td></tr> | |||
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=611:N-[(E)-3-[(2R,3S,4R,5S)-3,4-DIHYDROXY-5-PYRIDIN-4-YLSULFANYL-OXOLAN-2-YL]PROP-2-ENYL]-2,3-DIHYDROXY-5-NITRO-BENZAMIDE'>611</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</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=3oe5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3oe5 OCA], [https://pdbe.org/3oe5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3oe5 RCSB], [https://www.ebi.ac.uk/pdbsum/3oe5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3oe5 ProSAT]</span></td></tr> | |||
</table> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/COMT_RAT COMT_RAT] 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. | |||
==See Also== | |||
*[[Catechol O-methyltransferase 3D structures|Catechol O-methyltransferase 3D structures]] | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Large Structures]] | |||
[[Category: Rattus norvegicus]] | |||
[[Category: Benz J]] | |||
[[Category: Ehler A]] | |||
[[Category: Rudolph MG]] | |||
[[Category: Schlatter D]] | |||
[[Category: Stihle M]] | |||
Latest revision as of 11:16, 21 February 2024
Rat catechol O-methyltransferase in complex with a catechol-type, pyridylsulfanyl-containing inhibitor - humanized form
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