Crystal structure of albaflavenone monooxygenase containing a moonlighting terpene synthase active site (Q24657001)

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Crystal Structure of Albaflavenone Monooxygenase Containing a Moonlighting Terpene Synthase Active Site

Language	Label	Description	Also known as
English	Crystal structure of albaflavenone monooxygenase containing a moonlighting terpene synthase active site	scientific article	Crystal Structure of Albaflavenone Monooxygenase Containing a Moonlighting Terpene Synthase Active Site

Statements

scholarly article

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Crystal structure of albaflavenone monooxygenase containing a moonlighting terpene synthase active site (English)

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crystal structure

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ChEBI release 2020-05-28

author name string

Bin Zhao

1

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Li Lei

2

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Dmitry G Vassylyev

3

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Xin Lin

4

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David E Cane

5

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Steven L Kelly

6

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Hang Yuan

7

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David C Lamb

8

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Michael R Waterman

9

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language of work or name

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publication date

25 December 2009

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Journal of Biological Chemistry

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284

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52

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36711-9

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Identification of sesquiterpene synthases from Nostoc punctiforme PCC 73102 and Nostoc sp. strain PCC 7120

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7 April 2017

Biosynthesis of the sesquiterpene antibiotic albaflavenone in Streptomyces coelicolor A3(2)

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7 April 2017

Biosynthesis of the earthy odorant geosmin by a bifunctional Streptomyces coelicolor enzyme

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Adaptations for the oxidation of polycyclic aromatic hydrocarbons exhibited by the structure of human P450 1A2

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X-ray Crystal Structure of Aristolochene Synthase from Aspergillus terreus and Evolution of Templates for the Cyclization of Farnesyl Diphosphate † , ‡

1 reference

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Structure of trichodiene synthase from Fusarium sporotrichioides provides mechanistic inferences on the terpene cyclization cascade

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Crystal Structure of Pentalenene Synthase: Mechanistic Insights on Terpenoid Cyclization Reactions in Biology

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Structural Basis for Cyclic Terpene Biosynthesis by Tobacco 5-Epi-Aristolochene Synthase

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Crystal structure of recombinant farnesyl diphosphate synthase at 2.6-A resolution

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THE CARBON MONOXIDE-BINDING PIGMENT OF LIVER MICROSOMES. I. EVIDENCE FOR ITS HEMOPROTEIN NATURE

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Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2)

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Bacterial volatiles: the smell of small organisms

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28 September 2017

Structural biology and chemistry of the terpenoid cyclases

1 reference

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28 September 2017

Genome mining in Streptomyces coelicolor: molecular cloning and characterization of a new sesquiterpene synthase

1 reference

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Biosynthesis of plant volatiles: nature's diversity and ingenuity

1 reference

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1 reference

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Bifunctional and moonlighting enzymes: lighting the way to regulatory control

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Interdomain Communications in Bifunctional Enzymes: How Are Different Activities Coordinated?

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Enzymes with extra talents: moonlighting functions and catalytic promiscuity

1 reference

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Alteration of product formation by directed mutagenesis and truncation of the multiple-product sesquiterpene synthases delta-selinene synthase and gamma-humulene synthase

1 reference

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Production and characterization of bifunctional enzymes. Domain swapping to produce new bifunctional enzymes in the aspartate pathway

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28 September 2017

Moonlighting proteins.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2794785

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The cytochrome P450 gene family CYP157 does not contain EXXR in the K-helix reducing the absolute conserved P450 residues to a single cysteine.

1 reference

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21 January 2018

Do current sequence analysis algorithms disclose multifunctional (moonlighting) proteins?

1 reference

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21 January 2018

Structure and NTPase activity of the RNA-translocating protein (P4) of bacteriophage phi 6.

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Isolation and identification of allelochemicals that attract the larval parasitoid,Cotesia marginiventris (Cresson), to the microhabitat of one of its hosts.

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21 January 2018

Trans-β-farnesene, Alarm Pheromone of the Green Peach Aphid, Myzus persicae (Sulzer)

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12 December 2020

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https://pubmed.ncbi.nlm.nih.gov/19858213

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Odor-active alcohols from the fungal transformation of alpha-farnesene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19858213

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https://pubmed.ncbi.nlm.nih.gov/19858213

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https://pubmed.ncbi.nlm.nih.gov/19858213

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Identifiers

10.1074/JBC.M109.064683

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