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Journal Abstract Search

188 related items for PubMed ID: 23408308

  • 1. Conformational preferences of modified nucleoside N(4)-acetylcytidine, ac4C occur at "wobble" 34th position in the anticodon loop of tRNA.
    Kumbhar BV, Kamble AD, Sonawane KD.
    Cell Biochem Biophys; 2013 Jul; 66(3):797-816. PubMed ID: 23408308
    [Abstract] [Full Text] [Related]

  • 2. Structural significance of hypermodified nucleic acid base hydroxywybutine (OHyW) which occur at 37th position in the anticodon loop of yeast tRNA(Phe).
    Kumbhar NM, Kumbhar BV, Sonawane KD.
    J Mol Graph Model; 2012 Sep; 38():174-85. PubMed ID: 23073221
    [Abstract] [Full Text] [Related]

  • 3. Conformational Preferences of Modified Nucleoside 5-Taurinomethyluridine, τm(5)U Occur at 'wobble' 34th Position in the Anticodon Loop of tRNA.
    Kamble AS, Kumbhar BV, Sambhare SB, Bavi RS, Sonawane KD.
    Cell Biochem Biophys; 2015 Apr; 71(3):1589-603. PubMed ID: 25388845
    [Abstract] [Full Text] [Related]

  • 4. Conformational preferences and structural analysis of hypermodified nucleoside, peroxywybutosine (o2yW) found at 37th position in anticodon loop of tRNAPhe and its role in modulating UUC codon-anticodon interactions.
    Fandilolu PM, Kamble AS, Sambhare SB, Sonawane KD.
    Gene; 2018 Jan 30; 641():310-325. PubMed ID: 29107006
    [Abstract] [Full Text] [Related]

  • 5. Conformational preferences of hypermodified nucleoside lysidine (k2C) occurring at "wobble" position in anticodon loop of tRNA(Ile).
    Sonawane KD, Tewari R.
    Nucleosides Nucleotides Nucleic Acids; 2008 Oct 30; 27(10):1158-74. PubMed ID: 18788046
    [Abstract] [Full Text] [Related]

  • 6. Conformational preferences of modified nucleoside N(2)-methylguanosine (m(2)G) and its derivative N(2), N(2)-dimethylguanosine (m(2)(2)G) occur at 26th position (hinge region) in tRNA.
    Bavi RS, Kamble AD, Kumbhar NM, Kumbhar BV, Sonawane KD.
    Cell Biochem Biophys; 2011 Dec 30; 61(3):507-21. PubMed ID: 21735129
    [Abstract] [Full Text] [Related]

  • 7. Iso-energetic multiple conformations of hypermodified nucleic acid base wybutine (yW) which occur at 37(th) position in anticodon loop of tRNA(Phe).
    Kumbhar NM, Sonawane KD.
    J Mol Graph Model; 2011 Jun 30; 29(7):935-46. PubMed ID: 21530341
    [Abstract] [Full Text] [Related]

  • 8. The influence of hypermodified nucleosides lysidine and t(6)A to recognize the AUA codon instead of AUG: a molecular dynamics simulation study.
    Sonawane KD, Sambhare SB.
    Integr Biol (Camb); 2015 Nov 30; 7(11):1387-95. PubMed ID: 26215455
    [Abstract] [Full Text] [Related]

  • 9. Unconventional decoding of the AUA codon as methionine by mitochondrial tRNAMet with the anticodon f5CAU as revealed with a mitochondrial in vitro translation system.
    Takemoto C, Spremulli LL, Benkowski LA, Ueda T, Yokogawa T, Watanabe K.
    Nucleic Acids Res; 2009 Apr 30; 37(5):1616-27. PubMed ID: 19151083
    [Abstract] [Full Text] [Related]

  • 10. The RNA acetyltransferase driven by ATP hydrolysis synthesizes N4-acetylcytidine of tRNA anticodon.
    Ikeuchi Y, Kitahara K, Suzuki T.
    EMBO J; 2008 Aug 20; 27(16):2194-203. PubMed ID: 18668122
    [Abstract] [Full Text] [Related]

  • 11. Structural Significance of Conformational Preferences and Ribose-Ring-Puckering of Hyper Modified Nucleotide 5'-Monophosphate 2-Methylthio Cyclic N6-Threonylcarbamoyladenosine (p-ms2ct6A) Present at 37th Position in Anticodon Loop of tRNALys.
    Dound AS, Fandilolu PM, Sonawane KD.
    Cell Biochem Biophys; 2022 Dec 20; 80(4):665-680. PubMed ID: 35965304
    [Abstract] [Full Text] [Related]

  • 12. Conformational preferences of the base substituent in hypermodified nucleotide queuosine 5'-monophosphate 'pQ' and protonated variant 'pQH+'.
    Sonavane UB, Sonawane KD, Tewari R.
    J Biomol Struct Dyn; 2002 Dec 20; 20(3):473-85. PubMed ID: 12437386
    [Abstract] [Full Text] [Related]

  • 13. The human mitochondrial tRNAMet: structure/function relationship of a unique modification in the decoding of unconventional codons.
    Bilbille Y, Gustilo EM, Harris KA, Jones CN, Lusic H, Kaiser RJ, Delaney MO, Spremulli LL, Deiters A, Agris PF.
    J Mol Biol; 2011 Feb 18; 406(2):257-74. PubMed ID: 21168417
    [Abstract] [Full Text] [Related]

  • 14. tRNA's wobble decoding of the genome: 40 years of modification.
    Agris PF, Vendeix FA, Graham WD.
    J Mol Biol; 2007 Feb 09; 366(1):1-13. PubMed ID: 17187822
    [Abstract] [Full Text] [Related]

  • 15. Synthesis and investigation of the 5-formylcytidine modified, anticodon stem and loop of the human mitochondrial tRNAMet.
    Lusic H, Gustilo EM, Vendeix FA, Kaiser R, Delaney MO, Graham WD, Moye VA, Cantara WA, Agris PF, Deiters A.
    Nucleic Acids Res; 2008 Nov 09; 36(20):6548-57. PubMed ID: 18927116
    [Abstract] [Full Text] [Related]

  • 16. Conformational preferences of anticodon 3'-adjacent hypermodified nucleic acid base cis-or trans-zeatin and its 2-methylthio derivative, cis-or trans- ms(2)zeatin.
    Sonawane KD, Sonavane UB, Tewari R.
    J Biomol Struct Dyn; 2002 Feb 09; 19(4):637-48. PubMed ID: 11843625
    [Abstract] [Full Text] [Related]

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  • 18. Modifications modulate anticodon loop dynamics and codon recognition of E. coli tRNA(Arg1,2).
    Cantara WA, Bilbille Y, Kim J, Kaiser R, Leszczyńska G, Malkiewicz A, Agris PF.
    J Mol Biol; 2012 Mar 02; 416(4):579-97. PubMed ID: 22240457
    [Abstract] [Full Text] [Related]

  • 19. Solution structure of psi32-modified anticodon stem-loop of Escherichia coli tRNAPhe.
    Cabello-Villegas J, Nikonowicz EP.
    Nucleic Acids Res; 2005 Mar 02; 33(22):6961-71. PubMed ID: 16377777
    [Abstract] [Full Text] [Related]

  • 20. The effect of queuosine on tRNA structure and function.
    Morris RC, Brown KG, Elliott MS.
    J Biomol Struct Dyn; 1999 Feb 02; 16(4):757-74. PubMed ID: 10217448
    [Abstract] [Full Text] [Related]

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