「Pyrimidine」の共起表現(2語右で並び替え)

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共起表現

「Pyrimidine」の共起表現一覧(2語右で並び替え)

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er of 2',3'‐dideoxy‐3'‐thiacytidine and is a	pyrimidine nucleoside analogue.
Thus, the two substrates of this enzyme are	pyrimidine nucleoside and H2O, whereas its two products
Thus, the two substrates of this enzyme are	pyrimidine 5'-nucleotide and H2O, whereas its two produ
Thus, the two substrates of this enzyme are	pyrimidine nucleoside and phosphate, whereas its two pr
ydropyrimidine hydrase, hydantoin peptidase,	pyrimidine hydrase, and D-hydantoinase.
This enzyme participates in	pyrimidine metabolism and one carbon pool by folate.
in 3 metabolic pathways: purine metabolism,	pyrimidine metabolism, and bladder cancer.
d upstream of a variety of genes involved in	pyrimidine biosynthesis and transport.
dine is ribose (a pentose sugar) joined to a	pyrimidine base and is similar to cytidine, uridine, 2-
It is from UMP that other	pyrimidine nucleotides are derived.
The various purine and	pyrimidine bases are linked to the backbone by methylen
	Pyrimidine analogues are antimetabolites which mimic th
higher score to transitions (changes from a	pyrimidine such as C or T to another pyrimidine, or fro
enzyme participates in 3 metabolic pathways:	pyrimidine metabolism, beta-alanine metabolism, and pan
enzyme participates in 3 metabolic pathways:	pyrimidine metabolism, beta-alanine metabolism, and pan
it also catalyzes the preceding reaction in	pyrimidine nucleotide biosynthesis, the transfer of rib
related classes of molecules resembling the	pyrimidine nucleotides found in DNA.
Uridine triphosphate, which is a	pyrimidine nucleotide, has the ability to act as an ene
	Pyrimidine synthesis inhibitors are used in active mode
uridine (abbreviated as D, DHU, or UH2) is a	pyrimidine which is the result of adding two hydrogen a
Other names in common use include	pyrimidine ribonucleoside kinase, uridine-cytidine kina
yase (photosensitive), and deoxyribonucleate	pyrimidine dimer lyase (photosensitive).
kinase, ATP:UMP-CMP phosphotransferase, and	pyrimidine nucleoside monophosphate kinase.
Other names in common use include	pyrimidine nucleotide N-ribosidase, and Pyr5N.
se include N-ribosylpyrimidine nucleosidase,	pyrimidine nucleosidase, N-ribosylpyrimidine ribohydrol
is position should contain the complementary	pyrimidine, and not also be a purine.
	Pyrimidine biosynthesis occurs both in the body and thr
nce of hydrogen bonds between the purine and	pyrimidine bases of DNA were crucial to Watson and Cric
group is usually attached to carbon 5 of the	pyrimidine ring of uracil and cytosine.
phosphate fragment while the β-subunit binds	pyrimidine fragment of TPP, forming together a catalyti
ts as a coenzyme in the synthesis of purine,	pyrimidine and other amino acids.
occurs with carbamoyl phosphate entering the	pyrimidine synthesis pathway.
Because of the asymmetry in	pyrimidine and purine use in coding sequences, the stra
ine is a chemical compound composed of fused	pyrimidine and pyrazine rings.
of the azine series have (such as pyridine,	pyrimidine, pyridazine, pyrazine, 1,3,5-triazine and te
By inhibiting the formation of precursor	pyrimidine nucleotides, raltitrexed prevents the format
cur, which results in the elimination of the	pyrimidine dimer, returning it to its original state.
	Pyrimidine nucleotide synthesis starts with the formati
Isocytosine or 2-aminouracil is a	pyrimidine base that is an isomer of cytosine.
(or CTP synthetase) is an enzyme involved in	pyrimidine biosynthesis that interconverts UTP and CTP.
ssential coenzyme synthesised by coupling of	pyrimidine and thiazole moieties in bacteria.
Other names in common use include	pyrimidine phosphorylase, thymidine-orthophosphate deox
dehydrogenase, dihydrothymine dehydrogenase,	pyrimidine reductase, thymine reductase, uracil reducta
Other names in common use include	pyrimidine phosphorylase, UrdPase, UPH, and UPase.
HCFU (1-hexylcarbamoyl-5-fluorouracil) is a	pyrimidine analogue used as an antineoplastic agent.
ation in DNA that has neither a purine nor a	pyrimidine base, usually due to DNA damage.
"Synthesis of C-5 substituted	pyrimidine nucleosides via organopalladium intermediate
e (OMP), also known as orotidylic acid, is a	pyrimidine nucleotide which is the last intermediate in
lly at phosphodiester linkages adjacent to a	pyrimidine nucleotide, yielding 5'-phosphate-terminated

共起表現

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「Pyrimidine」の共起表現一覧(2語右で並び替え)