4.2.1.78: (S)-norcoclaurine synthase
This is an abbreviated version!
For detailed information about (S)-norcoclaurine synthase, go to the full flat file.
Word Map on EC 4.2.1.78
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4.2.1.78
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nanocrystals
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nerve
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nanoclusters
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photoluminescence
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nanoparticles
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colloidal
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fabric
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semiconductor
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luminescence
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nanocomposites
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perovskite
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neuropathy
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optoelectronic
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halide
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tunable
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dope
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nanostructures
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excitons
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as-prepared
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doping
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monodisperse
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nanomaterials
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electrocatalytic
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bimetallic
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sural
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photocatalytic
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dopants
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photothermal
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carpal
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photovoltaic
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ulnar
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light-emitting
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alloy
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nanocapsules
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bioimaging
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polyneuropathy
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core-shell
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photoelectron
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nanocubes
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photocatalysts
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hrtem
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electrocatalysts
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solvothermal
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ultrasmall
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heterostructures
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tunability
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synthesis
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vacancy
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radiative
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as-synthesized
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photocurrent
- 4.2.1.78
-
nanocrystals
- nerve
-
nanoclusters
-
photoluminescence
- nanoparticles
-
colloidal
-
fabric
-
semiconductor
-
luminescence
-
nanocomposites
-
perovskite
- neuropathy
-
optoelectronic
- halide
-
tunable
-
dope
-
nanostructures
-
excitons
-
as-prepared
-
doping
-
monodisperse
-
nanomaterials
-
electrocatalytic
-
bimetallic
-
sural
-
photocatalytic
-
dopants
-
photothermal
-
carpal
-
photovoltaic
-
ulnar
-
light-emitting
-
alloy
-
nanocapsules
-
bioimaging
- polyneuropathy
-
core-shell
-
photoelectron
-
nanocubes
-
photocatalysts
-
hrtem
-
electrocatalysts
-
solvothermal
-
ultrasmall
-
heterostructures
-
tunability
- synthesis
-
vacancy
-
radiative
-
as-synthesized
-
photocurrent
Reaction
Synonyms
(S)-norcoclaurine synthase, (S)-Norlaudanosoline synthase, AmNCS1, AmNCS2, CCHNCS2, CjNCS1, CjPR10A, CsNCS, More, NCS, NCS1, NCS2, NDONCS3, norcoclaurine synthase, PbNCS, PR10A, PSONCS1, PSONCS2, S-norcoclaurine synthase, Synthase, (S)-norlaudanosoline, TFLNCSDELTA25, TfNCS
ECTree
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Reaction
Reaction on EC 4.2.1.78 - (S)-norcoclaurine synthase
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4-hydroxyphenylacetaldehyde + dopamine = (S)-norcoclaurine + H2O
the reaction makes a 6-membered ring by forming a bond between C-6 of the 3,4-dihydroxyphenyl group of the dopamine and C-1 of the aldehyde in the imine formed between the substrates
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4-hydroxyphenylacetaldehyde + dopamine = (S)-norcoclaurine + H2O
the reaction makes a six-membered ring by forming a bond between C-6 of the 3,4-dihydroxyphenyl group of the dopamine and C-1 of the aldehyde in the imine formed between the substrates, the product is the precursor of the benzylisoquinoline alkaloids in plants, the enzyme, formerly known as (S)-norleudanosoline synthase, will also catalyse the reaction of 4-(2-aminoethyl)benzene-1,2-diol + (di-3,4-hydroxyphenyl)acetaldehyde to form (S)-norlaudanosoline, but this alkaloid has not been found to occur in plants, cooperativity between substrate binding sites
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4-hydroxyphenylacetaldehyde + dopamine = (S)-norcoclaurine + H2O
the reaction makes a six-membered ring by forming a bond between C-6 of the 3,4-dihydroxyphenyl group of the dopamine and C-1 of the aldehyde in the imine formed between the substrates, the product is the precursor of the benzylisoquinoline alkaloids in plants, the enzyme, formerly known as (S)-norleudanosoline synthase, will also catalyse the reaction of 4-(2-aminoethyl)benzene-1,2-diol + (di-3,4-hydroxyphenyl)acetaldehyde to form (S)-norlaudanosoline, but this alkaloid has not been found to occur in plants, cooperativity between substrate binding sites
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4-hydroxyphenylacetaldehyde + dopamine = (S)-norcoclaurine + H2O
the reaction makes a six-membered ring by forming a bond between C-6 of the 3,4-dihydroxyphenyl group of the dopamine and C-1 of the aldehyde in the imine formed between the substrates, the product is the precursor of the benzylisoquinoline alkaloids in plants, the enzyme, formerly known as (S)-norleudanosoline synthase, will also catalyse the reaction of 4-(2-aminoethyl)benzene-1,2-diol + (di-3,4-hydroxyphenyl)acetaldehyde to form (S)-norlaudanosoline, but this alkaloid has not been found to occur in plants, cooperativity between substrate binding sites
Thalictrum flavum ssp. glaucum
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4-hydroxyphenylacetaldehyde + dopamine = (S)-norcoclaurine + H2O
the reaction makes a six-membered ring by forming a bond between C-6 of the 3,4-dihydroxyphenyl group of the dopamine and C-1 of the aldehyde in the imine formed between the substrates, the product is the precursor of the benzylisoquinoline alkaloids in plants, the enzyme, formerly known as (S)-norleudanosoline synthase, will also catalyse the reaction of 4-(2-aminoethyl)benzene-1,2-diol + (di-3,4-hydroxyphenyl)acetaldehyde to form (S)-norlaudanosoline, but this alkaloid has not been found to occur in plants, iso-ordered bi-uni mechanism with 4-hydroxyphenylacetaldehyde binding before dopamine
Thalictrum flavum ssp. glaucum
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