「GLYCINE」の共起表現(1語右で並び替え)

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共起表現

「GLYCINE」の共起表現一覧(1語右で並び替え)

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ollagen, which is made up of lysine, proline,	glycine, alanine, and other amino acids .
Among them were aspartic acid, glutamic acid,	glycine, alanines, and butyric acid.
It has a lower negative charge than	glycine allowing it to migrate faster.
ting synthesis involving defects in arginine:	glycine amidinotransference and guanidinoacetate meth
contains hydroxyproline, serine, alanine and	glycine amino acids predominantly.
use include glutamic-glyoxylic transaminase,	glycine aminotransferase, glyoxylate-glutamic transam
that silk fibroin, known to consist mainly of	glycine and alanine, had a sequence of glycine-alanin
acid is a tripeptide composed of L-arginine,	glycine, and L-aspartic acid.
	Glycine and chiral (R-)valine are converted to a cycl
te, L-threo-3-phenylserine, and two products,	glycine and benzaldehyde.
hro-3-hydroxy-Ls-aspartate, and two products,	glycine and glyoxylate.
one substrate, L-threonine, and two products,	glycine and acetaldehyde.
acetate and H2O, whereas its two products are	glycine and urea.
Thus, the two substrates of this enzyme are	glycine and 2-oxoglutarate, whereas its two products
Thus, the two substrates of this enzyme are	glycine and A, whereas its 3 products are hydrogen cy
tral nervous system, the inhibitory action of	glycine and some of the action of GABA relies on the
The 3 substrates of this enzyme are ATP,	glycine, and tRNA(Gly), whereas its 3 products are AM
s division, second officer of the minesweeper	Glycine and manoeuvring-officer of the carrier Foch.
uence, mainly consisting of highly repetitive	glycine and alanine blocks, why silks are often refer
is produced by the enzyme ALA synthase, from	glycine and succinyl CoA.
at it consisted of four chains (two ending in	glycine and two ending in phenylalanine), with the ch
aving a higher degree of urinary excretion of	glycine and imino acids correlating to mutations in b
oth renal and intestinal transport systems of	glycine and imino acids.
d of nicotinic acetylcholine, GABAA, GABAA-ρ,	glycine and 5-HT3 receptors that are composed of five
es the carrier-mediated transport of choline,	glycine, and taurine, the function of delayed rectifi
ALA synthase removes the carboxyl group from	glycine and the CoA from the succinate by means of it
nding site of the neurotransmitter glutamate;	glycine antagonists, which bind to and block the glyc
High levels of plasma glutamine and	glycine are observed.
	Glycine betaine aldehyde, often simply called betaine
	Glycine betaine aldehyde is a short chain aldehyde an
This substance is now often called	glycine betaine to distinguish it from other betaines
	Glycine betaine aldehyde is a component of glycine, s
pounds are present in osmolytes, specifically	glycine betaine, which stabilize osmotic pressure in
tes the transformation of betaine aldehyde to	glycine betaine.
amylcysteine, which is readily condensed with	glycine, by glutathione synthetase, to form glutathio
Sarcosine is metabolized to	glycine by the enzyme sarcosine dehydrogenase, while
ine/adrenaline, dopamine, serotonin, proline,	glycine, choline, betaine and taurine.
This reaction, and by extension the	glycine cleavage system, is required for photorespira
The	glycine cleavage system is composed of four proteins:
role, and indeed a weak association with the	glycine cleavage system was observed.
The	glycine cleavage system catalyzes the degradation of
	Glycine cleavage in the photorespiratory pathway.
The	glycine cleavage system is also known as the glycine
GABA -	glycine co-release.
Elevation of extracellular synaptic	glycine concentration by blockade of GlyT1 has been h
The amino acid	glycine contributes all its carbon (2) and nitrogen (
	Glycine decarboxylase is a P-protein of the glycine c
Positive cooperativity would allow genes for	glycine degradation to be turned on more efficiently
nd upstream of the gcvT operon which controls	glycine degradation.
or the	glycine dehydroganse (cyanide forming)(EC 1.4.99.5).
the	glycine dehydrogenase (decarboxylating), which is ano
In enzymology, a	glycine dehydrogenase (cyanide-forming) (EC 1.4.99.5)
or the	glycine dehydrogenase (cytochrome) (EC 1.4.2.1).
In enzymology, a	glycine dehydrogenase (EC 1.4.1.10)
Allylglycine is a	glycine derivative.
N-Acetylglycinamide is a	glycine derivative.
	Glycine encephalopathy may be due to a defect in any
	Glycine encephalopathy, also known as "non-ketotic hy
overy is significant to the debate on whether	glycine exists widely in the universe.
acceptor, and H2O, whereas its 3 products are	glycine, formaldehyde, and reduced acceptor.
in which the carboxylic acid of the terminal	glycine from the di-glycine motif in the activated ub
s for monoamines, the amino acids proline and	glycine, GABA, and a group of orphan transporters.
ich this class of compounds can be related is	glycine, H2NCH2CO2H, in which the amino group, NH2,is
The 3 substrates of this enzyme are	glycine, H2O, and NAD+, whereas its 4 products are gl
primary amines, and the Gabriel synthesis of	glycine has yields as high as 85%.
ine domains (beta sheets) of the nano fibril,	glycine, having larger side groups, is mostly found i
cific for alanine, asparagine, aspartic acid,	glycine, histidine, lysine, phenylalanine, proline, s
and zinc on particle filtration and uptake of	glycine in the pacific oyster, Crassostrea gigas.
Also, type-IV lacks the regular	glycine in every third residue necessary for the tigh
mine (or guanidinoacetate) is a metabolite of	glycine in which the amino group has been converted i
It is thought that when	glycine is in excess it will bind to both aptamers to
in reacts with hot, dilute hydrochloric acid,	glycine is one of the products.
Hyperglycinemia refers to a condition where	glycine is elevated in the blood.
In it	glycine is a substrate, valine a chiral auxiliary and
Degradation of	glycine is brought about by the glycine cleavage syst
	Glycine levels in a bacterial cell must be maintained
The larvae feed on	Glycine max and Pueraria lobata.
abaceae, Lamiaceae, Malvaceae, Ranunculaceae,	Glycine max and Phaseolus vulgaris.
o the pterocarpans, are found in the soybean (	Glycine max) and have been found to have an antifunga
It is a phytoalexin found in the soybean (	Glycine max).
rduus horridulum, Heracleum maximum, Cuscuta,	Glycine max, Vicia faba, Verbascum thapsus, Juncus, P
from the experiments indicated that tyrosine,	glycine, methionine, and acetate are the primary prec
Other names in common use include	glycine methyltransferase, S-adenosyl-L-methionine:gl
atic name of this enzyme class is choloyl-CoA:	glycine N-choloyltransferase. Other names in common u
In enzymology, a	glycine N-methyltransferase (EC 2.1.1.20)
	Glycine neurotransmitter transporter, type 1 (SLC6A9)
	Glycine or acetate account for C-4 and C-5 on the pyr
AT2 is the high-affinity renal transporter of	glycine, proline and hydroxyproline found to be defec
ic proteins with high proportions of alanine,	glycine, proline, and glutamic acid.
robial flora, while the included pyruvate and	glycine promote the growth of Staphylococci.
ne, NAD+, and H2O, whereas its 4 products are	glycine, pyruvate, NADH, and H+.
It inhibits	glycine receptor activity, which decreases motor func
	Glycine receptor subunit alpha-2 is a protein that in
	Glycine receptor antagonists
It acts as a potent antagonist of the	glycine receptor, and has powerful convulsant effects
It is used in scientific research into the	glycine receptor, and is also sometimes associated wi
e GABAA receptor antagonist and also inhibits	glycine receptors with similar potency and nicotinic
(or inverse agonists) at either the GABAA or	glycine receptors, or ionotropic glutamate receptor a
ioredoxin reductases, formate dehydrogenases,	glycine reductases, and some hydrogenases).
It is more common on	glycine residues but also occurs on other amino acids
ionally, for example when previously internal	glycine residues become exposed by caspase cleavage d
ransferase (NMT), and occurs most commonly on	glycine residues exposed during co-translational N-te
to be ubiquitin (truncated by two C-terminal	glycine residues).
ogen bond donors are the peptide NH groups of	glycine residues.
Examples of the	glycine riboswitch exhibit sigmoidal binding curves w
The bacterial	glycine riboswitch is an RNA element that can bind th
	Glycine riboswitches usually consist of two metabolit
e "tandem arrangements" are also exhibited by	glycine riboswitches and TPP riboswitches where they
This enzyme participates in	glycine, serine and threonine metabolism and aminoacy
This enzyme participates in	glycine, serine and threonine metabolism and glyoxyla
This enzyme participates in	glycine, serine and threonine metabolism and glycerop
This enzyme participates in	glycine, serine and threonine metabolism and vitamin
enzyme participates in 4 metabolic pathways:	glycine, serine and threonine metabolism, cysteine me
s: urea cycle and metabolism of amino groups,	glycine, serine and threonine metabolism, histidine m
This enzyme participates in	glycine, serine and threonine metabolism.
nship with several other metabolic processes:	glycine, serine, and threonine metabolism which provi
se of excess urinary excretion of proline and	glycine, similar to that found in iminoglycinuria, is
MDA receptor (NMDAR) antagonist acting at the	glycine site on the NMDAR complex.
n NMDA antagonist, binding selectively to the	glycine site on the NMDA receptor complex, rather tha
lglycine, is an intermediate and byproduct in	glycine synthesis and degradation.
The P protein binds the alpha-amino group of	glycine through its pyridoxal phosphate cofactor.
rine, which, in turn, can create cysteine and	glycine through the homocysteine cycle.
The aptamers cooperatively bind	glycine to regulate the expression of downstream gene
he condensation of gamma-glutamylcysteine and	glycine, to form glutathione.
nature of the carboxyl-nitrogen bond) allows	glycine to assume this title.
In enzymology, a	glycine transaminase (EC 2.6.1.4)
Sodium- and chloride-dependent	glycine transporter 1 is a protein that in humans is
that is primarily made up of the amino acids	glycine, valine, alanine, and proline.
	Glycine watch (Swiss)
substrates of this enzyme are choloyl-CoA and	glycine, whereas its two products are CoA and glycoch
of this enzyme are S-adenosyl methionine and	glycine, whereas its two products are S-adenosylhomoc
yme are ATP, gamma-L-glutamyl-L-cysteine, and	glycine, whereas its 3 products are ADP, phosphate, a
hen abstracted from the prochiral position on	glycine with the aid of BuLi.
acid (dALA) by the reaction of the amino acid	glycine with succinyl-CoA from the citric acid cycle.

共起表現

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「GLYCINE」の共起表現一覧(1語右で並び替え)