These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 18635009)

  • 61. Regiospecific benzylation of tryptophan and derivatives catalyzed by a fungal dimethylallyl transferase.
    Liebhold M; Li SM
    Org Lett; 2013 Nov; 15(22):5834-7. PubMed ID: 24188078
    [TBL] [Abstract][Full Text] [Related]  

  • 62. A new member of the DMATS superfamily from Aspergillus niger catalyzes prenylations of both tyrosine and tryptophan derivatives.
    Fan A; Chen H; Wu R; Xu H; Li SM
    Appl Microbiol Biotechnol; 2014 Dec; 98(24):10119-29. PubMed ID: 24970457
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Enzymatic formation of a prenyl β-carboline by a fungal indole prenyltransferase.
    Hamdy SA; Kodama T; Nakashima Y; Han X; Matsui T; Morita H
    J Nat Med; 2022 Sep; 76(4):873-879. PubMed ID: 35767141
    [TBL] [Abstract][Full Text] [Related]  

  • 64. NovQ is a prenyltransferase capable of catalyzing the addition of a dimethylallyl group to both phenylpropanoids and flavonoids.
    Ozaki T; Mishima S; Nishiyama M; Kuzuyama T
    J Antibiot (Tokyo); 2009 Jul; 62(7):385-92. PubMed ID: 19557032
    [TBL] [Abstract][Full Text] [Related]  

  • 65. CdpC2PT, a reverse prenyltransferase from Neosartorya fischeri with a distinct substrate preference from known C2-prenyltransferases.
    Mundt K; Li SM
    Microbiology (Reading); 2013 Oct; 159(Pt 10):2169-2179. PubMed ID: 23845975
    [TBL] [Abstract][Full Text] [Related]  

  • 66. New insights into the biosynthesis of prenylated xanthones: Xptb from Aspergillus nidulans catalyses an O-prenylation of xanthones.
    Pockrandt D; Ludwig L; Fan A; König GM; Li SM
    Chembiochem; 2012 Dec; 13(18):2764-71. PubMed ID: 23150454
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Molecular analysis of a 4-dimethylallyltryptophan synthase from Malbranchea aurantiaca.
    Ding Y; Williams RM; Sherman DH
    J Biol Chem; 2008 Jun; 283(23):16068-76. PubMed ID: 18390548
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Enzymatic degradation of beta- and mixed alpha,beta-oligopeptides.
    Heck T; Limbach M; Geueke B; Zacharias M; Gardiner J; Kohler HP; Seebach D
    Chem Biodivers; 2006 Dec; 3(12):1325-48. PubMed ID: 17193247
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Reaction of the indole group with malondialdehyde: application for the derivatization of tryptophan residues in peptides.
    Foettinger A; Melmer M; Leitner A; Lindner W
    Bioconjug Chem; 2007; 18(5):1678-83. PubMed ID: 17705413
    [TBL] [Abstract][Full Text] [Related]  

  • 70. A new group of aromatic prenyltransferases in fungi, catalyzing a 2,7-dihydroxynaphthalene 3-dimethylallyl-transferase reaction.
    Haug-Schifferdecker E; Arican D; Brückner R; Heide L
    J Biol Chem; 2010 May; 285(22):16487-94. PubMed ID: 20351110
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Kinetics of the interaction of sulfate and hydrogen phosphate radicals with small peptides of glycine, alanine, tyrosine and tryptophan.
    Bosio G; Criado S; Massad W; Rodríguez Nieto FJ; Gonzalez MC; García NA; Mártire DO
    Photochem Photobiol Sci; 2005 Oct; 4(10):840-6. PubMed ID: 16189561
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Arabidopsis indole synthase, a homolog of tryptophan synthase alpha, is an enzyme involved in the Trp-independent indole-containing metabolite biosynthesis.
    Zhang R; Wang B; Ouyang J; Li J; Wang Y
    J Integr Plant Biol; 2008 Sep; 50(9):1070-7. PubMed ID: 18844775
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Nitrosation of N-terminally blocked tryptophan and tryptophan-containing peptides by peroxynitrite.
    Peyrot F; Ducrocq C
    Chembiochem; 2007 Jan; 8(2):217-23. PubMed ID: 17183522
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Prenylation of flavonoids by using a dimethylallyltryptophan synthase, 7-DMATS, from Aspergillus fumigatus.
    Yu X; Li SM
    Chembiochem; 2011 Oct; 12(15):2280-3. PubMed ID: 23106077
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Structural Basis of Tryptophan Reverse N-Prenylation Catalyzed by CymD.
    Roose BW; Christianson DW
    Biochemistry; 2019 Jul; 58(30):3232-3242. PubMed ID: 31251043
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Structure and function of cis-prenyl chain elongating enzymes.
    Takahashi S; Koyama T
    Chem Rec; 2006; 6(4):194-205. PubMed ID: 16900467
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Catalysts for the Enzymatic Lipidation of Peptides.
    Zheng Y; Cong Y; Schmidt EW; Nair SK
    Acc Chem Res; 2022 May; 55(9):1313-1323. PubMed ID: 35442036
    [TBL] [Abstract][Full Text] [Related]  

  • 78. An enzyme catalyzing O-prenylation of the glucose moiety of fusicoccin A, a diterpene glucoside produced by the fungus Phomopsis amygdali.
    Noike M; Liu C; Ono Y; Hamano Y; Toyomasu T; Sassa T; Kato N; Dairi T
    Chembiochem; 2012 Mar; 13(4):566-73. PubMed ID: 22287087
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Enzymatic investigation of the Staphylococcus aureus type I signal peptidase SpsB - implications for the search for novel antibiotics.
    Rao S; Bockstael K; Nath S; Engelborghs Y; Anné J; Geukens N
    FEBS J; 2009 Jun; 276(12):3222-34. PubMed ID: 19438721
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Catalytic potential of a fungal indole prenyltransferase toward β-carbolines, harmine and harman, and their prenylation effects on antibacterial activity.
    Hamdy SA; Kodama T; Nakashima Y; Han X; Morita H
    J Biosci Bioeng; 2022 Oct; 134(4):311-317. PubMed ID: 35931602
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.