Examining Reaction Specificity in PvcB, a Source of Diversity in Isonitrile-Containing Natural Products-Reference-Cited by-同舟云学术

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Examining Reaction Specificity in PvcB, a Source of Diversity in Isonitrile-Containing Natural Products

Published:2015-04-20 Issue:16 Volume:54 Page:2659-2669
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Zhu Jing¹,Lippa Geoffrey M.²,Gulick Andrew M.²³,Tipton Peter A.¹

Affiliation:

1. Department of Biochemistry, University of Missouri, Columbia, Missouri 65211, United States

2. Hauptman-Woodward Medical Research Foundation, Buffalo, New York 14203, United States

3. Department of Structural Biology, University at Buffalo, Buffalo, New York 14203, United States

Funder

Division of Molecular and Cellular Biosciences

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.biochem.5b00255

Reference32 articles.

1. Comparative analysis of hapalindole, ambiguine and welwitindolinone gene clusters and reconstitution of indole-isonitrile biosynthesis from cyanobacteria

2. Isocyanides and cyanides as natural products

3. Natural Products from isnA-Containing Biosynthetic Gene Clusters Recovered from the Genomes of Cultured and Uncultured Bacteria

4. Cloning and Heterologous Expression of Isocyanide Biosynthetic Genes from Environmental DNA

5. Non-Heme Fe(IV)–Oxo Intermediates

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1. Elucidation of divergent desaturation pathways in the formation of vinyl isonitrile and isocyanoacrylate;Nature Communications;2022-09-12

2. Medicinal Chemistry of Isocyanides;Chemical Reviews;2021-07-01

3. Biocatalysts from cyanobacterial hapalindole pathway afford antivirulent isonitriles against MRSA;Journal of Biosciences;2021-04-20

4. Current Understanding toward Isonitrile Group Biosynthesis and Mechanism;Chinese Journal of Chemistry;2021-01-27

5. Pathway from N‐Alkylglycine to Alkylisonitrile Catalyzed by Iron(II) and 2‐Oxoglutarate‐Dependent Oxygenases;Angewandte Chemie;2020-03-10

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