BRENDA - Enzyme Database show
show all sequences of 1.3.1.86

Multiple pathways for acetate assimilation in Streptomyces cinnamonensis

Akopiants, K.; Florova, G.; Li, C.; Reynolds, K.A.; J. Ind. Microbiol. Biotechnol. 33, 141-150 (2006)

Data extracted from this reference:

Organism
Organism
Primary Accession No. (UniProt)
Commentary
Textmining
Streptomyces cinnamonensis
-
strain C730.1
-
Substrates and Products (Substrate)
Substrates
Commentary Substrates
Literature (Substrates)
Organism
Products
Commentary (Products)
Literature (Products)
Organism (Products)
Reversibility
(E)-but-2-enoyl-CoA + NADPH + H+
-
712641
Streptomyces cinnamonensis
butanoyl-CoA + NADP+
-
-
-
?
Cofactor
Cofactor
Commentary
Organism
Structure
NADPH
-
Streptomyces cinnamonensis
Cofactor (protein specific)
Cofactor
Commentary
Organism
Structure
NADPH
-
Streptomyces cinnamonensis
Substrates and Products (Substrate) (protein specific)
Substrates
Commentary Substrates
Literature (Substrates)
Organism
Products
Commentary (Products)
Literature (Products)
Organism (Products)
Reversibility
(E)-but-2-enoyl-CoA + NADPH + H+
-
712641
Streptomyces cinnamonensis
butanoyl-CoA + NADP+
-
-
-
?
General Information
General Information
Commentary
Organism
physiological function
CCR and the butyryl-CoA pathway provide the majority of methylmalonyl-CoA and ethylmalonyl-CoA for monensin A biosynthesis
Streptomyces cinnamonensis
General Information (protein specific)
General Information
Commentary
Organism
physiological function
CCR and the butyryl-CoA pathway provide the majority of methylmalonyl-CoA and ethylmalonyl-CoA for monensin A biosynthesis
Streptomyces cinnamonensis
Other publictions for EC 1.3.1.86
No.
1st author
Pub Med
title
organims
journal
volume
pages
year
Activating Compound
Application
Cloned(Commentary)
Crystallization (Commentary)
Engineering
General Stability
Inhibitors
KM Value [mM]
Localization
Metals/Ions
Molecular Weight [Da]
Natural Substrates/ Products (Substrates)
Organic Solvent Stability
Organism
Oxidation Stability
Posttranslational Modification
Purification (Commentary)
Reaction
Renatured (Commentary)
Source Tissue
Specific Activity [micromol/min/mg]
Storage Stability
Substrates and Products (Substrate)
Subunits
Temperature Optimum [C]
Temperature Range [C]
Temperature Stability [C]
Turnover Number [1/s]
pH Optimum
pH Range
pH Stability
Cofactor
Ki Value [mM]
pI Value
IC50 Value
Activating Compound (protein specific)
Application (protein specific)
Cloned(Commentary) (protein specific)
Cofactor (protein specific)
Crystallization (Commentary) (protein specific)
Engineering (protein specific)
General Stability (protein specific)
IC50 Value (protein specific)
Inhibitors (protein specific)
Ki Value [mM] (protein specific)
KM Value [mM] (protein specific)
Localization (protein specific)
Metals/Ions (protein specific)
Molecular Weight [Da] (protein specific)
Natural Substrates/ Products (Substrates) (protein specific)
Organic Solvent Stability (protein specific)
Oxidation Stability (protein specific)
Posttranslational Modification (protein specific)
Purification (Commentary) (protein specific)
Renatured (Commentary) (protein specific)
Source Tissue (protein specific)
Specific Activity [micromol/min/mg] (protein specific)
Storage Stability (protein specific)
Substrates and Products (Substrate) (protein specific)
Subunits (protein specific)
Temperature Optimum [C] (protein specific)
Temperature Range [C] (protein specific)
Temperature Stability [C] (protein specific)
Turnover Number [1/s] (protein specific)
pH Optimum (protein specific)
pH Range (protein specific)
pH Stability (protein specific)
pI Value (protein specific)
Expression
General Information
General Information (protein specific)
Expression (protein specific)
KCat/KM [mM/s]
KCat/KM [mM/s] (protein specific)
725287
Aboulnaga
Effect of an Oxygen-Tolerant B ...
Clostridioides difficile
J. Bacteriol.
195
3704-3713
2013
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4
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1
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1
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1
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1
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1
1
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4
4
712235
Liu
Biosynthesis of salinosporamid ...
Salinispora tropica
J. Am. Chem. Soc.
131
10376-10377
2009
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712641
Akopiants
Multiple pathways for acetate ...
Streptomyces cinnamonensis
J. Ind. Microbiol. Biotechnol.
33
141-150
2006
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1
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656737
Li
Crotonyl-coenzyme A reductase ...
Streptomyces cinnamonensis, Streptomyces collinus
Microbiology
150
3463-3472
2004
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1
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4
4
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711366
Fukui
Engineering of Ralstonia eutro ...
Streptomyces cinnamonensis
Biomacromolecules
3
618-624
2002
1
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712939
Liu
Precursor supply for polyketid ...
Streptomyces cinnamonensis
Metab. Eng.
3
40-48
2001
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712617
Sun
-
Crotonic acid-directed biosynt ...
Streptomyces hygroscopicus subsp. ascomyceticus
J. Ferment. Bioeng.
86
261-265
1998
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713435
Stassi
Ethyl-substituted erythromycin ...
Streptomyces collinus
Proc. Natl. Acad. Sci. USA
95
7305-7309
1998
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1
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1
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712233
Liu
-
Linking diversity in evolution ...
Streptomyces collinus
J. Am. Chem. Soc.
119
2973-2979
1997
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712270
Han
A novel alternate anaplerotic ...
Streptomyces collinus
J. Bacteriol.
179
5157-5164
1997
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5
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711884
Wallace
Purification of crotonyl-CoA r ...
Streptomyces collinus
Eur. J. Biochem.
233
954-962
1995
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1
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19
2
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19
6
2
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711170
Dodds
-
Effects of coenzyme A and pH o ...
Bos taurus
Biochem. Soc. Trans.
9
556-557
1981
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390850
Strom
-
Activation and inhibition of c ...
Bos taurus
J. Biol. Chem.
254
8159-8162
1979
1
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390852
Maitra
Crotonyl coenzyme A reductase ...
Bos taurus
J. Biol. Chem.
249
111-117
1974
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2
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