9doj
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Influenza A virus polymerase PA subunit endonuclease domain bound to inhibitor Compound 19a== | |
+ | <StructureSection load='9doj' size='340' side='right'caption='[[9doj]], [[Resolution|resolution]] 1.48Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[9doj]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Influenza_A_virus Influenza A virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9DOJ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9DOJ 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]] 1.48Å</td></tr> | ||
+ | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1A8U:(2aS,4aR,10bS,11S,12R)-4a-(2,2-difluoroethyl)-16-hydroxy-2-methyl-2,2a,3,4,4a,5,6,10b-octahydrobenzo[h]pyrido[1,2 1,6][1,2,4]triazino[2,3-a]quinoline-1,15-dione'>A1A8U</scene>, <scene name='pdbligand=MLI:MALONATE+ION'>MLI</scene>, <scene name='pdbligand=MN:MANGANESE+(II)+ION'>MN</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=9doj FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9doj OCA], [https://pdbe.org/9doj PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9doj RCSB], [https://www.ebi.ac.uk/pdbsum/9doj PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9doj ProSAT]</span></td></tr> | ||
+ | </table> | ||
+ | == Function == | ||
+ | [https://www.uniprot.org/uniprot/A0A075EM28_9INFA A0A075EM28_9INFA] Plays an essential role in viral RNA transcription and replication by forming the heterotrimeric polymerase complex together with PB1 and PB2 subunits. The complex transcribes viral mRNAs by using a unique mechanism called cap-snatching. It consists in the hijacking and cleavage of host capped pre-mRNAs. These short capped RNAs are then used as primers for viral mRNAs. The PB2 subunit is responsible for the binding of the 5' cap of cellular pre-mRNAs which are subsequently cleaved after 10-13 nucleotides by the PA subunit that carries the endonuclease activity.[HAMAP-Rule:MF_04063] | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | A novel, highly diastereoselective, and metal-free synthesis of multisubstituted piperidines via an S(N)1 approach is reported in this study. The method allows for the preparation of highly functionalized compounds with exceptional diastereomeric selectivities and consistently reproducible yields. These compounds are of significant interest due to their remarkable biological activities toward influenza endonuclease. | ||
- | + | Highly Diastereoselective Access to Densely Functionalized Piperidine Cores of Influenza Endonuclease Inhibitors via a Metal-Free S(N)1 Approach.,Zhang Y, Sun C, Guo L, Zhao K, Bennett F, Lam YH, Gao Q, Ruhl KE, Pirnot MT, Emmert MH, Hollenstein K, Eddins MJ, Su HP, Shao G, Song C, Lo MM, Peng F, Qi J, Crowley BM, McCauley JA, Price IR J Org Chem. 2025 Jan 17;90(2):1175-1179. doi: 10.1021/acs.joc.4c02379. Epub 2025 , Jan 2. PMID:39745425<ref>PMID:39745425</ref> | |
- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
- | [[Category: | + | </div> |
+ | <div class="pdbe-citations 9doj" style="background-color:#fffaf0;"></div> | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Influenza A virus]] | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Eddins MJ]] | ||
+ | [[Category: Hollenstein K]] | ||
+ | [[Category: Price IR]] | ||
+ | [[Category: Su HP]] |
Current revision
Influenza A virus polymerase PA subunit endonuclease domain bound to inhibitor Compound 19a
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