6chh

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(New page: '''Unreleased structure''' The entry 6chh is ON HOLD Authors: Babault, N., Liu, J., Jin, J. Description: Structure of human NNMT in complex with bisubstrate inhibitor MS2756 [[Category...)
Current revision (15:04, 4 October 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6chh is ON HOLD
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==Structure of human NNMT in complex with bisubstrate inhibitor MS2756==
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<StructureSection load='6chh' size='340' side='right'caption='[[6chh]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6chh]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=6b1a 6b1a]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6CHH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6CHH 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=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=F0P:(2~{S})-5-[2-(3-aminocarbonylphenyl)ethyl-[[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methyl]amino]-2-azanyl-pentanoic+acid'>F0P</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=6chh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6chh OCA], [https://pdbe.org/6chh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6chh RCSB], [https://www.ebi.ac.uk/pdbsum/6chh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6chh ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/NNMT_HUMAN NNMT_HUMAN] Catalyzes the N-methylation of nicotinamide and other pyridines to form pyridinium ions. This activity is important for biotransformation of many drugs and xenobiotic compounds.
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Nicotinamide N-methyltransferase (NNMT) catalyzes the N-methylation of pyridine-containing compounds using the cofactor S-5'-adenosyl-L-methionine (SAM) as the methyl group donor. Through the regulation of the levels of its substrates, cofactor, and products, NNMT plays important role in physiology and pathophysiology. Overexpression of NNMT has been implicated in various human diseases. Potent and selective small-molecule NNMT inhibitors are valuable chemical tools for testing biological and therapeutic hypotheses. However, very few NNMT inhibitors have been reported. Here, we describe the discovery of a bisubstrate NNMT inhibitor MS2734 (6), and characterization of this inhibitor in biochemical, biophysical, kinetic, and structural studies. Importantly, we obtained the first crystal structure of human NNMT in complex with a small-molecule inhibitor. The structure of the NNMT-6 complex has unambiguously demonstrated that 6 occupied both substrate and cofactor binding sites. The findings paved the way for developing more potent and selective NNMT inhibitors in the future.
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Authors: Babault, N., Liu, J., Jin, J.
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Discovery of Bisubstrate Inhibitors of Nicotinamide N-Methyltransferase (NNMT).,Babault N, Allali-Hassani A, Li F, Fan J, Yue A, Ju K, Liu F, Vedadi M, Liu J, Jin J J Med Chem. 2018 Jan 10. doi: 10.1021/acs.jmedchem.7b01422. PMID:29320176<ref>PMID:29320176</ref>
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Description: Structure of human NNMT in complex with bisubstrate inhibitor MS2756
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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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[[Category: Babault, N]]
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<div class="pdbe-citations 6chh" style="background-color:#fffaf0;"></div>
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[[Category: Liu, J]]
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== References ==
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[[Category: Jin, J]]
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Babault N]]
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[[Category: Jin J]]
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[[Category: Liu J]]

Current revision

Structure of human NNMT in complex with bisubstrate inhibitor MS2756

PDB ID 6chh

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