「phenylalanine」の共起表現(1語左で並び替え)

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共起表現

「phenylalanine」の共起表現一覧(1語左で並び替え)

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In enzymology, a	phenylalanine 2-monooxygenase (EC 1.13.12.9) is an enzym
In enzymology, a	phenylalanine adenylyltransferase (EC 2.7.7.54) is an en
Protegrin-4 substitutes a	phenylalanine for a valine at position 14 and sequences
In enzymology, a	phenylalanine N-acetyltransferase (EC 2.3.1.53)
an inability to break down the amino acid	phenylalanine due to an hereditary deficiency of the nec
strongly elevated levels of the amino acid	phenylalanine in the blood.
synthesized by plants from the amino acid	phenylalanine.
rotein composed entirely of the amino acid	phenylalanine.
RNA codons, which coded for the amino acid	phenylalanine.
mes, used in the degradation of amino acid	phenylalanine and in the biosynthesis of the neurotransm
idual components, including aspartic acid,	phenylalanine, methanol, and further breakdown products
e biosynthesis of the aromatic amino acids	phenylalanine and tyrosine.
The aromatic amino acids	phenylalanine and tyrosine
ase (deaminating and decarboxylating), and	phenylalanine (deaminating, decarboxylating)oxidase.
similar to the two amino acids alanine and	phenylalanine.
atic amino acids tyrosine, tryptophan, and	phenylalanine.
ve proteins after leucine, methionine, and	phenylalanine residues.
ylase (TPH), tyrosine hydroxylase (TH) and	phenylalanine hydroxylase (PAH) are members of a superfa
ine, isoleucine, methionine, tyrosine, and	phenylalanine.
me participates in tyrosine metabolism and	phenylalanine metabolism.
This enzyme participates in tyrosine and	phenylalanine catabolism.
"Xxx" is either an aromatic (	phenylalanine, tyrosine) or a branched aliphatic (valine
metabolism of aromatic amino acids such as	phenylalanine and tyrosine.
nd preferably aromatic amino acids such as	phenylalanine, tryptophan, and tyrosine.
ional homologs were uncovered that contain	phenylalanine codons instead of leucine codons, and are
amicidin A contains Tryptophan, B contains	Phenylalanine and C contains Tyrosine.
a centrally-acting inhibitor of the enzyme	phenylalanine hydroxylase (PH).
hesis is performed by action of the enzyme	phenylalanine ammonia-lyase (PAL) on phenylalanine.
In analogy to the enzymes	phenylalanine hydroxylase, tyrosine hydroxylase, tryptop
ic code is read in triplets, the codon for	phenylalanine is UUU.
ver, the body can synthesise tyrosine from	phenylalanine, an essential amino acid.
ants, ferulic acid (right) is derived from	phenylalanine, which is converted to 4-hydroxycinnamic a
f cinnamic acid, which is synthesized from	phenylalanine in the first step of phenylpropanoid biosy
ynthesized from tyrosine or a hydroxylated	phenylalanine.
This enzyme participates in	phenylalanine, tyrosine and tryptophan biosynthesis and
This enzyme participates in	phenylalanine, tyrosine and tryptophan biosynthesis and
This enzyme participates in	phenylalanine, tyrosine and tryptophan biosynthesis and
It is involved in	phenylalanine, tryptophan, and alkaloid production, and
With a special diet low in	phenylalanine, PKU newborns can grow and develop into no
form chorismate which can then be used in	phenylalanine, tyrosine or tryptophan biosynthesis.
s (two ending in glycine and two ending in	phenylalanine), with the chains cross-linked by disulfid
This enzyme participates in	phenylalanine metabolism.
This enzyme participates in	phenylalanine, tyrosine and tryptophan biosynthesis.
This enzyme participates in	phenylalanine metabolism and phenylpropanoid biosynthesi
This enzyme participates in	phenylalanine and tryptophan metabolism.
lps convert several amino acids, including	phenylalanine, to other essential molecules in the body.
enzyme found to use tetrahydrobiopterin is	phenylalanine hydroxylase (PAH).
d sequence is N-formylmethionine, leucine,	phenylalanine.
are derived from aromatic amino acids like	phenylalanine, tyrosine, tryptophan, and the thyroid hor
aspartic acid, glycine, histidine, lysine,	phenylalanine, proline, serine, and threonine belong to
ethionine metabolism, tyrosine metabolism,	phenylalanine metabolism, phenylalanine, tyrosine and tr
histidine metabolism, tyrosine metabolism,	phenylalanine metabolism, phenylalanine, tyrosine and tr
5 metabolic pathways: tyrosine metabolism,	phenylalanine metabolism, nitrogen metabolism, phenylpro
histidine metabolism, tyrosine metabolism,	phenylalanine metabolism, and metabolism of xenobiotics
histidine metabolism, tyrosine metabolism,	phenylalanine metabolism, tryptophan metabolism, beta-al
on-enzymatic free-radical hydroxylation of	phenylalanine under conditions of oxidative stress.
) that contains many codons for leucine or	phenylalanine.
P1 position) is a tyrosine, tryptophan, or	phenylalanine.
acids as are the aromatic amino acid pair,	phenylalanine and tyrosine.
and II cleave hemoglobin between residues	Phenylalanine 33 and Leucine 34 of α-globin subunit.
d by a special diet with highly restricted	phenylalanine content.
As a result,	phenylalanine from the diet builds up in the bloodstream
The	phenylalanine moiety is bound to the enzyme because of s
EA5 patients have a cysteine to	phenylalanine mutation at position 104.
Analogously to	phenylalanine hydroxylase and tyrosine hydroxylase, this
Other names in common use include tyrase,	phenylalanine deaminase, tyrosine ammonia-lyase, L-tyros
esis of the aromatic amino acids tyrosine,	phenylalanine, and tryptophan.

共起表現

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「phenylalanine」の共起表現一覧(1語左で並び替え)