4.2.1.20: tryptophan synthase
This is an abbreviated version!
For detailed information about tryptophan synthase, go to the full flat file.
Word Map on EC 4.2.1.20
-
4.2.1.20
-
pain
-
pyridoxal
-
typhimurium
-
myofascial
-
alpha-subunits
-
beta-subunits
-
5'-phosphate
-
aldimine
-
vanilloid
-
indole-3-glycerol
-
trapezius
-
nociceptive
-
nose
-
cone-shaped
-
melastatin
-
palpation
-
bienzyme
-
epiphyses
-
quinonoid
-
craniofacial
-
miles
-
pear-shaped
-
tension-type
-
polycystin
-
sternocleidomastoid
-
beta-site
-
tryptophanase
-
l-trp
-
urea-induced
-
temporalis
-
suboccipital
-
metacarpal
-
bulbous
-
phalanx
-
tryptophanyl-trna
-
taut
-
assessor
-
scapula
-
chaffeensis
-
indoline
-
ehrlichia
-
levator
-
5'-phosphate-dependent
-
eyebrows
-
masseter
-
dimethylallyl
-
trpcs
-
capitis
-
exostoses
-
polymodal
-
biotechnology
-
synthesis
-
analysis
- 4.2.1.20
- pain
- pyridoxal
- typhimurium
-
myofascial
- alpha-subunits
- beta-subunits
- 5'-phosphate
-
aldimine
-
vanilloid
-
indole-3-glycerol
-
trapezius
-
nociceptive
-
nose
-
cone-shaped
-
melastatin
-
palpation
-
bienzyme
-
epiphyses
-
quinonoid
-
craniofacial
- miles
-
pear-shaped
-
tension-type
-
polycystin
-
sternocleidomastoid
-
beta-site
- tryptophanase
- l-trp
-
urea-induced
-
temporalis
-
suboccipital
-
metacarpal
-
bulbous
-
phalanx
-
tryptophanyl-trna
-
taut
- assessor
-
scapula
- chaffeensis
- indoline
- ehrlichia
-
levator
-
5'-phosphate-dependent
-
eyebrows
-
masseter
-
dimethylallyl
-
trpcs
-
capitis
- exostoses
-
polymodal
- biotechnology
- synthesis
- analysis
Reaction
Synonyms
alpha2beta2 tryptophan synthase, alphaTS, AtTSB1, beta subunit of tryptophan synthase, indoleglycerol phosphate aldolase, It-TSA, L-serine hydro-lyase (adding indoleglycerol-phosphate), L-tryptophan synthetase, PtTSA, Rv1612, synthase, tryptophan, TrB, Trp synthase, Trp synthase beta, TrpA, trpB, TrpB1, TrpB2, TrpB2a, TrpB2i, TrpB2o, TRPS, tryptophan desmolase, tryptophan synthase, tryptophan synthase alpha subunit, tryptophan synthase alpha-subunit, tryptophan synthase alpha2beta2 complex, tryptophan synthase beta, tryptophan synthase beta 1, tryptophan synthase beta subunit, tryptophan synthetase, TS, TSA, TSase, TSB, TSB1, TSbeta
ECTree
Advanced search results
Application
Application on EC 4.2.1.20 - tryptophan synthase
Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
analysis
-
the enzyme complex is a model enzyme for understanding allosteric regulation
biotechnology
-
enzyme is a target for structure-based design of herbicides
synthesis
-
Recycling of hair by acid hydrolysis has enormous economic importance. Enzymatic synthesis of L-tryptophan from hair acid hydrolysis industries wastewater with tryptophan synthase. The L-serine conversion rate reaches 95.1% with a final L-tryptophan concentration of 33.2 g/l
synthesis
-
synthesis of L-2-methyltryptophan L-serine and 2-methylindole by recombinant Escherichia coli with tryptophan synthase activity. Under the optimal conditions including 100 mmol/l L-serine, 100 mmol/l 2-methylindole, 1 g tryptophan synthase cells, 0.1mmol/l Ca2+, 50 ml reaction volume, 37ºC, pH 8.0, the bioconversion rate of L-2-methyltryptophan reaches 93% after 6 h
synthesis
-
the reaction of mutant L166V with L-amino acid oxidase, halogenase enzymes and palladium chemocatalysts provides access to further D-configured and regioselectively halogenated or arylated beta-methyltryptophan derivatives
synthesis
use of enzyme in production of psilocybin formation from 4-hydroxyindole and L-serine, and similarly of 7-phosphoryloxytryptamine (isonorbaeocystin), and of serotonin, together with Psilocybe cubensis enzymes PsiD, PsiK, and PsiM, which provide decarboxylase, kinase, and methyltransferase activity, respectively
synthesis
-
Recycling of hair by acid hydrolysis has enormous economic importance. Enzymatic synthesis of L-tryptophan from hair acid hydrolysis industries wastewater with tryptophan synthase. The L-serine conversion rate reaches 95.1% with a final L-tryptophan concentration of 33.2 g/l
-
synthesis
-
the reaction of mutant L166V with L-amino acid oxidase, halogenase enzymes and palladium chemocatalysts provides access to further D-configured and regioselectively halogenated or arylated beta-methyltryptophan derivatives
-