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4lvg

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'''Unreleased structure'''
 
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The entry 4lvg is ON HOLD
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==Fragment-based Identification of Amides Derived From trans-2-(Pyridin-3-yl)cyclopropanecarboxylic Acid as Potent Inhibitors of Human Nicotinamide Phosphoribosyltransferase (NAMPT)==
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<StructureSection load='4lvg' size='340' side='right'caption='[[4lvg]], [[Resolution|resolution]] 1.70&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4lvg]] 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=4LVG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4LVG 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]] 1.702&#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=20O:(1S,2S)-N-[4-(PHENYLSULFONYL)PHENYL]-2-(PYRIDIN-3-YL)CYCLOPROPANECARBOXAMIDE'>20O</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</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=4lvg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4lvg OCA], [https://pdbe.org/4lvg PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4lvg RCSB], [https://www.ebi.ac.uk/pdbsum/4lvg PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4lvg ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/NAMPT_HUMAN NAMPT_HUMAN] Catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to yield nicotinamide mononucleotide, an intermediate in the biosynthesis of NAD. It is the rate limiting component in the mammalian NAD biosynthesis pathway (By similarity).
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Authors: Giannetti, A.M., Zheng, X., Skelton, N., Wang, W., Bravo, B., Feng, Y., Gunzner-Toste, J., Ho, Y., Hua, R., Wang, C., Zhao, Q., Liederer, B.M., Liu, Y., O' Brien, T., Oeh, J., Sampath, D., Shen, Y., Wang, L., Wu, H., Xiao, Y., Yuen, P., Zak, M., Zhao, G., Dragovich, P.S.
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==See Also==
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*[[Phosphoribosyltransferase 3D structures|Phosphoribosyltransferase 3D structures]]
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Description: Fragment-based Identification of Amides Derived From trans-2-(Pyridin-3-yl)cyclopropanecarboxylic Acid as Potent Inhibitors of Human Nicotinamide Phosphoribosyltransferase (NAMPT)
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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: Bravo B]]
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[[Category: Dragovich PS]]
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[[Category: Feng Y]]
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[[Category: Giannetti AM]]
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[[Category: Gunzner-Toste J]]
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[[Category: Ho Y]]
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[[Category: Hua R]]
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[[Category: Liederer BM]]
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[[Category: Liu Y]]
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[[Category: O'Brien T]]
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[[Category: Oeh J]]
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[[Category: Sampath D]]
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[[Category: Shen Y]]
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[[Category: Skelton N]]
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[[Category: Wang C]]
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[[Category: Wang L]]
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[[Category: Wang W]]
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[[Category: Wu H]]
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[[Category: Xiao Y]]
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[[Category: Yuen P]]
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[[Category: Zak M]]
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[[Category: Zhao G]]
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[[Category: Zhao Q]]
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[[Category: Zheng X]]

Current revision

Fragment-based Identification of Amides Derived From trans-2-(Pyridin-3-yl)cyclopropanecarboxylic Acid as Potent Inhibitors of Human Nicotinamide Phosphoribosyltransferase (NAMPT)

PDB ID 4lvg

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