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Effects of Halide Ions on the Carbamidocyclophane Biosynthesis in Nostoc sp. CAVN2

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.200351947openalex-snapshot

Elimination of Zero‐Quantum Interference in Two‐Dimensional NMR Spectra

inferredcites →https://doi.org/10.1002/anie.201003500openalex-snapshot

Asymmetric Total Synthesis of Cylindrocyclophanes A and F through Cyclodimerization and a Ramberg–Bäcklund Reaction

inferredcites →https://doi.org/10.1002/anie.201005280openalex-snapshot

Tandem Acyl Carrier Proteins in the Curacin Biosynthetic Pathway Promote Consecutive Multienzyme Reactions with a Synergistic Effect

inferredcites →https://doi.org/10.1002/anie.201503186openalex-snapshot

Biosynthesis‐Assisted Structural Elucidation of the Bartolosides, Chlorinated Aromatic Glycolipids from Cyanobacteria

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Bromobalhimycin and Chlorobromobalhimycins—Illuminating the Potential of Halogenases in Glycopeptide Antibiotic Biosyntheses

inferredcites →https://doi.org/10.1002/cbic.201300345openalex-snapshot

More than just a Halogenase: Modification of Fatty Acyl Moieties by a Trifunctional Metal Enzyme

inferredcites →https://doi.org/10.1007/bf02825067openalex-snapshot

A simplified protocol for preparing DNA from filamentous cyanobacteria

inferredcites →https://doi.org/10.1007/s10811-015-0657-7openalex-snapshot

Impact of temperature on the biosynthesis of cytotoxically active carbamidocyclophanes A–E in Nostoc sp. CAVN10

inferredcites →https://doi.org/10.1007/s10811-015-0751-xopenalex-snapshot

Erratum to: Impact of temperature on the biosynthesis of cytotoxically active carbamidocyclophanes A–E in Nostoc sp. CAVN10

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Coherence transfer by isotropic mixing: Application to proton correlation spectroscopy

inferredcites →https://doi.org/10.1016/0022-2364(85)90018-6openalex-snapshot

MLEV-17-based two-dimensional homonuclear magnetization transfer spectroscopy

inferredcites →https://doi.org/10.1016/0022-2364(86)90091-0openalex-snapshot

Sensitivity-enhanced two-dimensional heteronuclear relayed coherence transfer NMR spectroscopy

inferredcites →https://doi.org/10.1016/0022-2364(86)90395-1openalex-snapshot

Sensitivity-enhanced two-dimensional heteronuclear shift correlation NMR spectroscopy

inferredcites →https://doi.org/10.1016/0022-2364(89)90153-4openalex-snapshot

Implementation of the DEPT sequence in inverse shift correlation; the DEPT-HMQC

inferredcites →https://doi.org/10.1016/0076-6879(88)67086-8openalex-snapshot

[83] Conjugal transfer of DNA to cyanobacteria

inferredcites →https://doi.org/10.1016/b978-008045382-8.00041-1openalex-snapshot

The Natural Products Chemistry of Cyanobacteria

inferredcites →https://doi.org/10.1016/j.chembiol.2004.03.030openalex-snapshot

Structure and Biosynthesis of the Jamaicamides, New Mixed Polyketide-Peptide Neurotoxins from the Marine Cyanobacterium Lyngbya majuscula

inferredcites →https://doi.org/10.1016/j.copbio.2010.09.019openalex-snapshot

Biologically active secondary metabolites from marine cyanobacteria

inferredcites →https://doi.org/10.1016/j.phytochem.2012.03.005openalex-snapshot

Merocyclophanes A and B, antiproliferative cyclophanes from the cultured terrestrial Cyanobacterium Nostoc sp.

inferredcites →https://doi.org/10.1016/j.tetlet.2013.11.112openalex-snapshot

Carbamidocyclophanes F and G with anti-Mycobacterium tuberculosis activity from the cultured freshwater cyanobacterium Nostoc sp.

inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot

Basic Local Alignment Search Tool

inferredcites →https://doi.org/10.1016/s0040-4020(01)00931-0openalex-snapshot

Marine cyanobacteria—a prolific source of natural products

inferredcites →https://doi.org/10.1016/s0040-4020(01)87237-9openalex-snapshot

Biosynthetic origin of [7.7]paracyclophanes from cyanobacteria

inferredcites →https://doi.org/10.1016/s0040-4020(01)92244-6openalex-snapshot

Structures of cylindrocyphanes a-f

inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00301openalex-snapshot

Combining Mass Spectrometric Metabolic Profiling with Genomic Analysis: A Powerful Approach for Discovering Natural Products from Cyanobacteria

inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00576openalex-snapshot

Brominated Variant of the Lantibiotic NAI-107 with Enhanced Antibacterial Potency

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Cylindrofridins A–C, Linear Cylindrocyclophane-Related Alkylresorcinols from the Cyanobacterium Cylindrospermum stagnale

inferredcites →https://doi.org/10.1021/ja000429qopenalex-snapshot

Total Synthesis of (−)-Cylindrocyclophane A via a Double Horner-Emmons Macrocyclic Dimerization Event

inferredcites →https://doi.org/10.1021/ja00166a066openalex-snapshot

[7.7]Paracyclophanes from blue-green algae

inferredcites →https://doi.org/10.1021/ja00268a061openalex-snapshot

Proton and carbon-13 assignments from sensitivity-enhanced detection of heteronuclear multiple-bond connectivity by 2D multiple quantum NMR

inferredcites →https://doi.org/10.1021/ja00362a038openalex-snapshot

Sensitivity-enhanced correlation of nitrogen-15 and proton chemical shifts in natural-abundance samples via multiple quantum coherence

inferredcites →https://doi.org/10.1021/ja00388a062openalex-snapshot

Multiple quantum filters for elucidating NMR coupling networks

inferredcites →https://doi.org/10.1021/ja0106164openalex-snapshot

Total Synthesis of (−)-Cylindrocyclophanes A and F Exploiting the Reversible Nature of the Olefin Cross Metathesis Reaction

inferredcites →https://doi.org/10.1021/ja01521a040openalex-snapshot

Biosynthesis of Tetracyclines. I. The Halide Metabolism of Streptomyces aureofaciens Mutants. The Preparation and Characterization of Tetracycline, 7-Chloro36 -tetracycline and 7-Bromotetracycline

inferredcites →https://doi.org/10.1021/ja308318popenalex-snapshot

Cylindrocyclophane Biosynthesis Involves Functionalization of an Unactivated Carbon Center

inferredcites →https://doi.org/10.1021/ja991538bopenalex-snapshot

Total Synthesis of (−)-Cylindrocyclophane F

inferredcites →https://doi.org/10.1021/jf9912708openalex-snapshot

Influence of Halogen Salts on the Production of the Ochratoxins by Aspergillus ochraceus Wilh.

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Structures of nostocyclophanes A-D

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Biosynthetic Pathway and Gene Cluster Analysis of Curacin A, an Antitubulin Natural Product from the Tropical Marine Cyanobacterium Lyngbya majuscula

inferredcites →https://doi.org/10.1021/np060324mopenalex-snapshot

Carbamidocyclophanes A−E, Chlorinated Paracyclophanes with Cytotoxic and Antibiotic Activity from the Vietnamese Cyanobacterium Nostoc sp.

inferredcites →https://doi.org/10.1021/np100352eopenalex-snapshot

Cylindrocyclophanes with Proteasome Inhibitory Activity from the Cyanobacterium Nostoc sp.

inferredcites →https://doi.org/10.1021/np800651mopenalex-snapshot

Biohalogenation: Nature’s Way to Synthesize Halogenated Metabolites

inferredcites →https://doi.org/10.1038/ja.2007.2openalex-snapshot

Effects of Halogens on the Production of Salinosporamides by the Obligate Marine Actinomycete Salinispora tropica

inferredcites →https://doi.org/10.1038/ja.2014.118openalex-snapshot

Anti-MRSA-acting carbamidocyclophanes H–L from the Vietnamese cyanobacterium Nostoc sp. CAVN2

inferredcites →https://doi.org/10.1039/b807243dopenalex-snapshot

Isoprenoid-like alkylations in polyketide biosynthesis

inferredcites →https://doi.org/10.1039/b909646aopenalex-snapshot

Syntheses of naturally occurring cytotoxic [7.7]paracyclophanes, (−)-cylindrocyclophane A and its enantiomer, and implications for biological activity

inferredcites →https://doi.org/10.1039/c4sc03132fopenalex-snapshot

Assembly line termination in cylindrocyclophane biosynthesis: discovery of an editing type II thioesterase domain in a type I polyketide synthase

inferredcites →https://doi.org/10.1055/s-0033-1338879openalex-snapshot

Using Chemical Knowledge to Uncover New Biological Function: Discovery of the Cylindrocyclophane Biosynthetic Pathway

inferredcites →https://doi.org/10.1073/pnas.1006738107openalex-snapshot

Conformational switch triggered by α-ketoglutarate in a halogenase of curacin A biosynthesis

inferredcites →https://doi.org/10.1073/pnas.74.12.5463openalex-snapshot

DNA sequencing with chain-terminating inhibitors

inferredcites →https://doi.org/10.1078/1438-4639-00045openalex-snapshot

Biochemical and pharmacological investigations of selected cyanobacteria

inferredcites →https://doi.org/10.1080/00021369.1969.10859317openalex-snapshot

Isolation of the Bromo Analogues of Pyrrolnitrin fromPseudomonas pyrrolnitrica

inferredcites →https://doi.org/10.1093/bioinformatics/btm091openalex-snapshot

Enhancements and modifications of primer design program Primer3

inferredcites →https://doi.org/10.1093/bioinformatics/btn548openalex-snapshot

Aggressive assembly of pyrosequencing reads with mates

inferredcites →https://doi.org/10.1093/bioinformatics/btq413openalex-snapshot

genoPlotR: comparative gene and genome visualization in R

inferredcites →https://doi.org/10.1093/bioinformatics/bts199openalex-snapshot

Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data

inferredcites →https://doi.org/10.1093/bioinformatics/btu031openalex-snapshot

InterProScan 5: genome-scale protein function classification

inferredcites →https://doi.org/10.1093/nar/gkf436openalex-snapshot

MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform

inferredcites →https://doi.org/10.1093/nar/gkg312openalex-snapshot

GenDB--an open source genome annotation system for prokaryote genomes

inferredcites →https://doi.org/10.1093/nar/gkl723openalex-snapshot

MetaGene: prokaryotic gene finding from environmental genome shotgun sequences

inferredcites →https://doi.org/10.1093/nar/gks596openalex-snapshot

Primer3—new capabilities and interfaces

inferredcites →https://doi.org/10.1093/nar/gku1243openalex-snapshot

The InterPro protein families database: the classification resource after 15 years

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inferredcites →https://doi.org/10.1186/1471-2105-11-119openalex-snapshot

Prodigal: prokaryotic gene recognition and translation initiation site identification

inferredcites →https://doi.org/10.1271/bbb1961.33.294openalex-snapshot

Isolation of the Bromo Analogues of Pyrrolnitrin from Pseudomonas pyrrolnitrica

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Antimicrobial and Anti-Inflammatory Activities of Endophytic Fungi Talaromyces wortmannii Extracts against Acne-Inducing Bacteria

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Halogenating Enzymes for Selective Halogenation Reactions

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Marinopyrrole Derivatives as Potential Antibiotic Agents against Methicillin-Resistant Staphylococcus aureus (I)

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Antibacterial and Cytotoxic New Napyradiomycins from the Marine-Derived Streptomyces sp. SCSIO 10428

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Marinopyrrole Derivatives as Potential Antibiotic Agents against Methicillin-Resistant Staphylococcus aureus (III)

inferredcites →https://doi.org/10.7164/antibiotics.36.1431openalex-snapshot

Pyrrolomycins F1,F2a,F2b and F3,new metabolites produced by the addition of bromide to the fermentation.

inferredcites →https://doi.org/10.7164/antibiotics.36.1735openalex-snapshot

The biosynthesis of brominated pyrrolnitrin derivatives by Pseudomonas aureofaciens.

inferredcites →https://doi.org/10.7164/antibiotics.39.487openalex-snapshot

Novel antibiotics napyradiomycins. Production, isolation, physico-chemical properties and biological activity.

inferredcites →https://doi.org/10.7164/antibiotics.42.1070openalex-snapshot

Calicheamicins, a novel family of antitumor antibiotics. 3. Isolation, purification and characterization of calicheamicins .BETA.1Br, .GAMMA.1Br, .ALPHA.2I, .ALPHA.3I, .BETA.1I, .GAMMA.1I and .DELTA.1I.

inferredcites →https://doi.org/10.7164/antibiotics.42.1299openalex-snapshot

New antitumor antibiotics, duocarmycins B1 and B2.

inferredcites →https://doi.org/10.7164/antibiotics.42.558openalex-snapshot

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inferredcites →https://doi.org/10.7164/antibiotics.53.1openalex-snapshot

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Biocatalytic Friedel–Crafts Alkylation Using a Promiscuous Biosynthetic Enzyme

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