Biosynthesis of terpenoids: YgbB protein converts 4-diphosphocytidyl-2C-methyl-D-erythritol 2-phosphate to 2C-methyl-D-erythritol 2,4-cyclodiphosphate (Q24678236)

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Language	Label	Description	Also known as
English	Biosynthesis of terpenoids: YgbB protein converts 4-diphosphocytidyl-2C-methyl-D-erythritol 2-phosphate to 2C-methyl-D-erythritol 2,4-cyclodiphosphate	scientific article

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scholarly article

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Biosynthesis of terpenoids: YgbB protein converts 4-diphosphocytidyl-2C-methyl-D-erythritol 2-phosphate to 2C-methyl-D-erythritol 2,4-cyclodiphosphate (English)

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1 reference

based on heuristic

inferred from title

Capsicum annuum

1 reference

(2S)-2-methylbutane-1,2,3,4-tetrol

1 reference

author name string

S Herz

1

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J Wungsintaweekul

2

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C A Schuhr

3

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S Hecht

4

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H Luttgen

5

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S Sagner

6

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M Fellermeier

7

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W Eisenreich

8

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M H Zenk

9

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A Bacher

10

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F Rohdich

11

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language of work or name

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publication date

14 March 2000

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Proceedings of the National Academy of Sciences of the United States of America

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97

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6

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2486-90

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online access status

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1073/pnas.040554697?email=unpaywall_01@example.com

access restriction status

1 reference

based on heuristic

inferred from online access status

Biosynthesis of terpenoids: YchB protein of Escherichia coli phosphorylates the 2-hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

7 April 2017

Cytidine 5'-triphosphate-dependent biosynthesis of isoprenoids: YgbP protein of Escherichia coli catalyzes the formation of 4-diphosphocytidyl-2-C-methylerythritol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

7 April 2017

A 1-deoxy-D-xylulose 5-phosphate reductoisomerase catalyzing the formation of 2-C-methyl-D-erythritol 4-phosphate in an alternative nonmevalonate pathway for terpenoid biosynthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

7 April 2017

Identification of a thiamin-dependent synthase in Escherichia coli required for the formation of the 1-deoxy-D-xylulose 5-phosphate precursor to isoprenoids, thiamin, and pyridoxol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

7 April 2017

The complete genome sequence of Escherichia coli K-12

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

7 April 2017

Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

7 April 2017

Cloning and characterization of a gene from Escherichia coli encoding a transketolase-like enzyme that catalyzes the synthesis of D-1-deoxyxylulose 5-phosphate, a common precursor for isoprenoid, thiamin, and pyridoxol biosynthesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

28 September 2017

A family of transketolases that directs isoprenoid biosynthesis via a mevalonate-independent pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

28 September 2017

Terpenoid biosynthesis from 1-deoxy-D-xylulose in higher plants by intramolecular skeletal rearrangement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

28 September 2017

Incorporation of 1-deoxy-D-xylulose into isoprene and phytol by higher plants and algae

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

28 September 2017

Structure determination of a novel cyclic phosphocompound isolated from Desulfovibrio desulfuricans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

30 May 2018

The ability of bacteria to synthesize a new cyclopyrophosphate correlates with their tolerance to redox-cycling drugs: on a crossroad of chemotherapy, environmental toxicology and immunobiochemical problems

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15955

30 May 2018

Dedicated roles of plastid transketolases during the early onset of isoprenoid biogenesis in pepper fruits1.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.040554697

21 January 2018

Isoprenoid biosynthesis via a mevalonate-independent pathway in plants: cloning and heterologous expression of 1-deoxy-D-xylulose-5-phosphate reductoisomerase from peppermint

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.040554697

21 January 2018

Cloning and heterologous expression of a cDNA encoding 1-deoxy-D-xylulose-5-phosphate reductoisomerase of Arabidopsis thaliana

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.040554697

21 January 2018

Mevalonate-Independent Biosynthesis of Terpenoid Volatiles in Plants: Induced and Constitutive Emission of Volatiles

1 reference

https://pubmed.ncbi.nlm.nih.gov/10694574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The deoxyxylulose phosphate pathway of terpenoid biosynthesis in plants and microorganisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/10694574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of oxidative stress on the biosynthesis of 2-C-methyl-D-erythritol-2,4-cyclopyrophosphate and isoprenoids by several bacterial strains

1 reference

https://pubmed.ncbi.nlm.nih.gov/10694574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.040554697

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2000PNAS...97.2486H

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PubMed publication ID

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