(Q36484013)

English

Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Unified biogenesis of ambiguine, fischerindole, hapalindole and welwitindolinone: identification of a monogeranylated indolenine as a cryptic common biosynthetic intermediate by an unusual magnesium-dependent aromatic prenyltransferase (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

3-geranyl-3-[(Z)-2-isocyanovinyl]-3H-indole

1 reference

ChEBI release 2020-05-28

3-[(Z)-2-isocyanovinyl]indole

1 reference

ChEBI release 2020-05-28

Matthew L. Hillwig

object named as

Matthew L Hillwig

2

0 references

Angela Gronenborn

object named as

Angela M Gronenborn

4

0 references

Leonardus M I Koharudin

3

object named as

Leonardus M I Koharudin

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

author name string

Xinyu Liu

1

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

language of work or name

0 references

publication date

7 January 2016

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Chemical Communications

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

52

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

1737-1740

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

The Chemistry of Hapalindoles, Fischerindoles, Ambiguines, and Welwitindolinones.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Terpenoid biosynthesis off the beaten track: unconventional cyclases and their impact on biomimetic synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Mechanistic studies on the indole prenyltransferases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

A new family of iron-dependent halogenases acts on freestanding substrates.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Prenyl transfer to aromatic substrates: genetics and enzymology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Indole prenyltransferases from fungi: a new enzyme group with high potential for the production of prenylated indole derivatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

The ABBA family of aromatic prenyltransferases: broadening natural product diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Antimicrobial ambiguines from the cyanobacterium Fischerella sp. collected in Israel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

CloQ, a prenyltransferase involved in clorobiocin biosynthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Structure, mechanism and function of prenyltransferases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Mapping protein-protein interactions in solution by NMR spectroscopy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Protein-protein interactions probed by nuclear magnetic resonance spectroscopy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

30 September 2017

Identification and characterization of a welwitindolinone alkaloid biosynthetic gene cluster in the stigonematalean Cyanobacterium Hapalosiphon welwitschii.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

28 June 2018

Total synthesis of hapalindole-type natural products.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

21 September 2018

Mechanism of dimethylallyltryptophan synthase: evidence for a dimethylallyl cation intermediate in an aromatic prenyltransferase reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

21 September 2018

Aromatic prenylation in phenazine biosynthesis: dihydrophenazine-1-carboxylate dimethylallyltransferase from Streptomyces anulatus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4720564

21 September 2018

Promiscuous indolyl vinyl isonitrile synthases in the biogenesis and diversification of hapalindole-type alkaloids.

1 reference

https://api.crossref.org/works/10.1039%2FC5CC10060G

21 January 2018

Rearrangement of 3,3-disubstituted indolenines and synthesis of 2,3-substituted indoles

1 reference

https://pubmed.ncbi.nlm.nih.gov/26740122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biosynthesis of ambiguine indole alkaloids in cyanobacterium Fischerella ambigua

1 reference

https://pubmed.ncbi.nlm.nih.gov/26740122

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1039/C5CC10060G

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

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