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 *

118 related articles for article (PubMed ID: 32412572)

  • 1. Mutational biosynthesis to generate novel analogs of nosiheptide featuring a fluorinated indolic acid moiety.
    Zhang E; Guo H; Chen D; Yang Q; Fan Y; Yin Y; Wang W; Chen D; Wang S; Liu W
    Org Biomol Chem; 2020 Jun; 18(21):4051-4055. PubMed ID: 32412572
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework.
    Yu Y; Duan L; Zhang Q; Liao R; Ding Y; Pan H; Wendt-Pienkowski E; Tang G; Shen B; Liu W
    ACS Chem Biol; 2009 Oct; 4(10):855-64. PubMed ID: 19678698
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biosynthesis of the nosiheptide indole side ring centers on a cryptic carrier protein NosJ.
    Ding W; Ji W; Wu Y; Wu R; Liu WQ; Mo T; Zhao J; Ma X; Zhang W; Xu P; Deng Z; Tang B; Yu Y; Zhang Q
    Nat Commun; 2017 Sep; 8(1):437. PubMed ID: 28874663
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mechanistic Insights into the Radical S-adenosyl-l-methionine Enzyme NosL From a Substrate Analogue and the Shunt Products.
    Ji X; Li Y; Jia Y; Ding W; Zhang Q
    Angew Chem Int Ed Engl; 2016 Mar; 55(10):3334-7. PubMed ID: 26837062
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Radical-mediated enzymatic carbon chain fragmentation-recombination.
    Zhang Q; Li Y; Chen D; Yu Y; Duan L; Shen B; Liu W
    Nat Chem Biol; 2011 Mar; 7(3):154-60. PubMed ID: 21240261
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Substrate-Tuned Catalysis of the Radical S-Adenosyl-L-Methionine Enzyme NosL Involved in Nosiheptide Biosynthesis.
    Ji X; Li Y; Ding W; Zhang Q
    Angew Chem Int Ed Engl; 2015 Jul; 54(31):9021-4. PubMed ID: 26138750
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Crystal structure of tryptophan lyase (NosL): evidence for radical formation at the amino group of tryptophan.
    Nicolet Y; Zeppieri L; Amara P; Fontecilla-Camps JC
    Angew Chem Int Ed Engl; 2014 Oct; 53(44):11840-4. PubMed ID: 25196319
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mechanistic Studies on the Radical SAM Enzyme Tryptophan Lyase (NosL).
    Bhandari DM; Fedoseyenko D; Begley TP
    Methods Enzymol; 2018; 606():155-178. PubMed ID: 30097091
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Capturing Intermediates in the Reaction Catalyzed by NosN, a Class C Radical S-Adenosylmethionine Methylase Involved in the Biosynthesis of the Nosiheptide Side-Ring System.
    Wang B; LaMattina JW; Marshall SL; Booker SJ
    J Am Chem Soc; 2019 Apr; 141(14):5788-5797. PubMed ID: 30865439
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Using peptide substrate analogs to characterize a radical intermediate in NosN catalysis.
    Wang B; Silakov A; Booker SJ
    Methods Enzymol; 2022; 666():469-487. PubMed ID: 35465928
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Radical S-Adenosylmethionine Protein NosN Forms the Side Ring System of Nosiheptide by Functionalizing the Polythiazolyl Peptide S-Conjugated Indolic Moiety.
    Qiu Y; Du Y; Wang S; Zhou S; Guo Y; Liu W
    Org Lett; 2019 Mar; 21(5):1502-1505. PubMed ID: 30785762
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reactivity of the nitrogen-centered tryptophanyl radical in the catalysis by the radical SAM enzyme NosL.
    Qianzhu H; Ji W; Ji X; Chu L; Guo C; Lu W; Ding W; Gao J; Zhang Q
    Chem Commun (Camb); 2016 Dec; 53(2):344-347. PubMed ID: 27929146
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Insights into quinaldic acid moiety formation in thiostrepton biosynthesis facilitating fluorinated thiopeptide generation.
    Duan L; Wang S; Liao R; Liu W
    Chem Biol; 2012 Apr; 19(4):443-8. PubMed ID: 22520750
    [TBL] [Abstract][Full Text] [Related]  

  • 14. NocU is a cytochrome P450 oxygenase catalyzing
    Guo H; Bai X; Yang Q; Xue Y; Chen D; Tao J; Liu W
    Org Biomol Chem; 2021 Oct; 19(38):8338-8342. PubMed ID: 34523664
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rerouting the Pathway for the Biosynthesis of the Side Ring System of Nosiheptide: The Roles of NosI, NosJ, and NosK.
    Badding ED; Grove TL; Gadsby LK; LaMattina JW; Boal AK; Booker SJ
    J Am Chem Soc; 2017 Apr; 139(16):5896-5905. PubMed ID: 28343381
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of truncated form of NosP as a transcription factor to regulate the biosynthesis of nosiheptide.
    Wu X; Jin L; Zhang H; Tong R; Ma M; Chen Y
    FASEB J; 2018 Jan; 32(1):453-465. PubMed ID: 28935819
    [TBL] [Abstract][Full Text] [Related]  

  • 17. NosN, a Radical S-Adenosylmethionine Methylase, Catalyzes Both C1 Transfer and Formation of the Ester Linkage of the Side-Ring System during the Biosynthesis of Nosiheptide.
    LaMattina JW; Wang B; Badding ED; Gadsby LK; Grove TL; Booker SJ
    J Am Chem Soc; 2017 Dec; 139(48):17438-17445. PubMed ID: 29039940
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutasynthesis Generates Antibacterial Benzothiophenic-Containing Nosiheptide Analogues.
    Mu N; Guo H; Zhang E; Yin Y; Wang W; Chen D; Wang S; Liu W
    J Nat Prod; 2022 Oct; 85(10):2274-2281. PubMed ID: 36122372
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Selective biosynthesis of a rhamnosyl nosiheptide by a novel bacterial rhamnosyltransferase.
    Du Y; Xia Y; Wu L; Chen L; Rong J; Fan J; Chen Y; Wu X
    Microb Biotechnol; 2024 Jan; 17(1):e14412. PubMed ID: 38265165
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reprogramming the Biosynthesis of Precursor Peptide to Create a Selenazole-Containing Nosiheptide Analogue.
    Tan Y; Wang M; Chen Y
    ACS Synth Biol; 2022 Jan; 11(1):85-91. PubMed ID: 35006674
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.