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Journal Abstract Search

167 related items for PubMed ID: 30251899

  • 1.
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  • 2. 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; 31(sup4):78-87. PubMed ID: 27578398
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  • 4. (31)P NMR studies of O-acetylserine sulfhydrylase-B from Salmonella typhimurium.
    Guan R, Nimmo SA, Schnackerz KD, Cook PF.
    Arch Biochem Biophys; 2009 Jul 15; 487(2):85-90. PubMed ID: 19501038
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  • 6. Cysteine 42 is important for maintaining an integral active site for O-acetylserine sulfhydrylase resulting in the stabilization of the alpha-aminoacrylate intermediate.
    Tai CH, Yoon MY, Kim SK, Rege VD, Nalabolu SR, Kredich NM, Schnackerz KD, Cook PF.
    Biochemistry; 1998 Jul 28; 37(30):10597-604. PubMed ID: 9692949
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  • 7. 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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  • 8. Kinetic mechanisms of the A and B isozymes of O-acetylserine sulfhydrylase from Salmonella typhimurium LT-2 using the natural and alternative reactants.
    Tai CH, Nalabolu SR, Jacobson TM, Minter DE, Cook PF.
    Biochemistry; 1993 Jun 29; 32(25):6433-42. PubMed ID: 8518286
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  • 10. Isozyme-specific ligands for O-acetylserine sulfhydrylase, a novel antibiotic target.
    Spyrakis F, Singh R, Cozzini P, Campanini B, Salsi E, Felici P, Raboni S, Benedetti P, Cruciani G, Kellogg GE, Cook PF, Mozzarelli A.
    PLoS One; 2013 Jun 29; 8(10):e77558. PubMed ID: 24167577
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  • 12. Crystal structure of O-Acetylserine sulfhydralase (OASS) isoform 3 from Entamoeba histolytica: Pharmacophore-based virtual screening and validation of novel inhibitors.
    Dharavath S, Vijayan R, Kumari K, Tomar P, Gourinath S.
    Eur J Med Chem; 2020 Apr 15; 192():112157. PubMed ID: 32145643
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  • 15. Structural insight into the interaction of O-acetylserine sulfhydrylase with competitive, peptidic inhibitors by saturation transfer difference-NMR.
    Benoni R, Pertinhez TA, Spyrakis F, Davalli S, Pellegrino S, Paredi G, Pezzotti A, Bettati S, Campanini B, Mozzarelli A.
    FEBS Lett; 2016 Apr 15; 590(7):943-53. PubMed ID: 27072053
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  • 17. Comparative thermodynamic studies on substrate and product binding of O-acetylserine sulfhydrylase reveals two different ligand recognition modes.
    Banerjee S, Ekka MK, Kumaran S.
    BMC Biochem; 2011 Jun 02; 12():31. PubMed ID: 21631959
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  • 18. Formation of the alpha-aminoacrylate immediate limits the overall reaction catalyzed by O-acetylserine sulfhydrylase.
    Woehl EU, Tai CH, Dunn MF, Cook PF.
    Biochemistry; 1996 Apr 16; 35(15):4776-83. PubMed ID: 8664267
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  • 19. 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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