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Journal Abstract Search

218 related items for PubMed ID: 19928859

  • 1. Design of O-acetylserine sulfhydrylase inhibitors by mimicking nature.
    Salsi E, Bayden AS, Spyrakis F, Amadasi A, Campanini B, Bettati S, Dodatko T, Cozzini P, Kellogg GE, Cook PF, Roderick SL, Mozzarelli A.
    J Med Chem; 2010 Jan 14; 53(1):345-56. PubMed ID: 19928859
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  • 2. Substrate-Induced Facilitated Dissociation of the Competitive Inhibitor from the Active Site of O-Acetyl Serine Sulfhydrylase Reveals a Competitive-Allostery Mechanism.
    Singh AK, Ekka MK, Kaushik A, Pandya V, Singh RP, Banerjee S, Mittal M, Singh V, Kumaran S.
    Biochemistry; 2017 Sep 19; 56(37):5011-5025. PubMed ID: 28805060
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  • 3. Fine tuning of the active site modulates specificity in the interaction of O-acetylserine sulfhydrylase isozymes with serine acetyltransferase.
    Spyrakis F, Felici P, Bayden AS, Salsi E, Miggiano R, Kellogg GE, Cozzini P, Cook PF, Mozzarelli A, Campanini B.
    Biochim Biophys Acta; 2013 Jan 19; 1834(1):169-81. PubMed ID: 23000429
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  • 5. Inhibition of O-acetylserine sulfhydrylase by fluoroalanine derivatives.
    Franko N, Grammatoglou K, Campanini B, Costantino G, Jirgensons A, Mozzarelli A.
    J Enzyme Inhib Med Chem; 2018 Dec 19; 33(1):1343-1351. PubMed ID: 30251899
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  • 7. Identification of cysteine metabolism regulator (CymR)-derived pentapeptides as nanomolar inhibitors of Staphylococcus aureus O-acetyl-ʟ-serine sulfhydrylase (CysK).
    Pederick JL, Vandborg BC, George A, Bovermann H, Boyd JM, Freundlich JS, Bruning JB.
    bioRxiv; 2024 Sep 20. PubMed ID: 39345565
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  • 11. Structure-Based Design of Inhibitors of the Crucial Cysteine Biosynthetic Pathway Enzyme O-Acetyl Serine Sulfhydrylase.
    Mazumder M, Gourinath S.
    Curr Top Med Chem; 2016 Sep 20; 16(9):948-59. PubMed ID: 26303427
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  • 12. The narrow active-site cleft of O-acetylserine sulfhydrylase from Leishmania donovani allows complex formation with serine acetyltransferases with a range of C-terminal sequences.
    Raj I, Kumar S, Gourinath S.
    Acta Crystallogr D Biol Crystallogr; 2012 Aug 20; 68(Pt 8):909-19. PubMed ID: 22868756
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  • 13. Cyclopropane-1,2-dicarboxylic acids as new tools for the biophysical investigation of O-acetylserine sulfhydrylases by fluorimetric methods and saturation transfer difference (STD) NMR.
    Annunziato G, Pieroni M, Benoni R, Campanini B, Pertinhez TA, Pecchini C, Bruno A, Magalhães J, Bettati S, Franko N, Mozzarelli A, Costantino G.
    J Enzyme Inhib Med Chem; 2016 Aug 20; 31(sup4):78-87. PubMed ID: 27578398
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  • 15. Advancements in inhibitors of crucial enzymes in the cysteine biosynthetic pathway: Serine acetyltransferase and O-acetylserine sulfhydrylase.
    Qin Y, Teng Y, Yang Y, Mao Z, Zhao S, Zhang N, Li X, Niu W.
    Chem Biol Drug Des; 2024 Jul 20; 104(1):e14573. PubMed ID: 38965664
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  • 16. Structural basis for interaction of O-acetylserine sulfhydrylase and serine acetyltransferase in the Arabidopsis cysteine synthase complex.
    Francois JA, Kumaran S, Jez JM.
    Plant Cell; 2006 Dec 20; 18(12):3647-55. PubMed ID: 17194764
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  • 17. Crystal structure of native O-acetyl-serine sulfhydrylase from Entamoeba histolytica and its complex with cysteine: structural evidence for cysteine binding and lack of interactions with serine acetyl transferase.
    Chinthalapudi K, Kumar M, Kumar S, Jain S, Alam N, Gourinath S.
    Proteins; 2008 Sep 20; 72(4):1222-32. PubMed ID: 18350570
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  • 19. Structure-based mutational studies of O-acetylserine sulfhydrylase reveal the reason for the loss of cysteine synthase complex formation in Brucella abortus.
    Dharavath S, Raj I, Gourinath S.
    Biochem J; 2017 Mar 23; 474(7):1221-1239. PubMed ID: 28126739
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