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1 ATHIONINE gamma-SYNTHASE (AtCGS), Met's main regulatory enzyme.
2 the molecular architecture of this important regulatory enzyme.
3 of structure-function relationships of this regulatory enzyme.
4 ct binding of a kinesin-related protein to a regulatory enzyme.
5 of acetyl-CoA carboxylase, a major upstream regulatory enzyme.
6 n of potent and selective inhibitors of this regulatory enzyme.
7 nit interactions, resulting in an allosteric regulatory enzyme.
8 operties and effector sensitivities of these regulatory enzymes.
9 biopterin (BH4) is a cofactor of a number of regulatory enzymes.
10 eomic approach, we identified the glycolytic regulatory enzyme, 6-phosphofructo-2-kinase/fructose-2,6
11 However, with the exception of a few key regulatory enzymes, a comprehensive and quantitative ass
12 y functional human E2 that mediated enhanced regulatory enzyme activities but, lacking E3BP, supporte
13 '-AMP, is a potent activator of an important regulatory enzyme, AMP-activated protein kinase (AMPK).
14 that HDAC3 represses the synthesis of a key regulatory enzyme and reveal a novel mechanism by which
16 ugh genetic analyses, we uncovered roles for regulatory enzymes and mitochondrial localization in the
17 ssociated with hyperlipidemia, altered lipid regulatory enzymes and receptors, and increased risk of
18 his issue, we examined the expression of S1P regulatory enzymes and S1P receptors during cardiac deve
19 sed to describe the allosteric properties of regulatory enzymes and subsequently extended to receptor
22 e self-association and activity of important regulatory enzymes, and examined conformational properti
24 e macromolecular complex suggests that these regulatory enzymes are coordinately positioned to regula
27 tone lactylation is installed and removed by regulatory enzymes as opposed to spontaneous chemical re
28 l, even though brain neurons express the key regulatory enzymes associated with building or burning g
29 ,4-trisphosphate 5/6-kinase (ITPK1) is a key regulatory enzyme at the branch point for the synthesis
30 moserine dehydrogenase (HSD) function as key regulatory enzymes at branch points in the aspartate ami
31 ntiation anti-cancer agents target chromatin regulatory enzymes buoyed early interest in developing d
32 encodes a member of the Pak family of actin-regulatory enzymes, but whose in vivo function is unknow
33 ing as both protein quality surveillance and regulatory enzymes by performing highly regulated proteo
34 ulations of MASS models explicitly show that regulatory enzymes can control dynamic states of network
35 Rare variants (RVs) in the gene encoding the regulatory enzyme complement factor I (CFI; FI) that red
36 dvances in our understanding of how PTMs and regulatory enzymes control the signaling activity of RLR
37 suggest the EGAP NAT complex is an essential regulatory enzyme controlling the function of a subset o
38 we demonstrate that prostaglandin E2 and its regulatory enzyme, COX-2, are also targets of Tpl2-trans
39 nthesis by increasing phosphorylation of the regulatory enzyme CTP:phosphocholine cytidylyltransferas
40 ectively inhibiting the activity of the rate-regulatory enzyme, CTP:phosphocholine cytdylyltransferas
41 ctivity in plants, and identified a critical regulatory enzyme, cytosolic phosphoribosyl pyrophosphat
43 is frequently considered vested in classical regulatory enzymes, each strongly displaced from equilib
44 Protein kinases constitute a large family of regulatory enzymes, each with a distinct specificity to
45 to the coupling cation Na(+) and also to the regulatory enzyme EIIA(Glc) of the glucose-specific phos
46 enerated by glucosylceramide synthase, a key regulatory enzyme encoded by the UDP-glucose ceramide gl
47 hat S. mutans ADP-Glc PPase is an allosteric regulatory enzyme exhibiting sensitivity to modulation b
48 ine cytidylyltransferase (Pcyt2) is the main regulatory enzyme for de novo biosynthesis of phosphatid
49 he expression of ent-kaurene synthase, a key regulatory enzyme for gibberellin synthesis, the followi
50 ee-fold increase in the activity of the rate-regulatory enzyme for PC synthesis, cytidylyltransferase
52 '-phosphate hydrolase has been proposed as a regulatory enzyme for vitamin B-6, but we found B-6 vita
54 r structural principles operate in bacterial regulatory enzymes, gene repressors (and the related nuc
55 a mechanism through which a single chromatin regulatory enzyme has the ability to sense chemical micr
56 il now the identity or the function of these regulatory enzymes has not been defined in any crop plan
59 ndritic cells (DCs) competent to express the regulatory enzyme IDO in mice are a small but distinctiv
60 inactivate GS kinase-3beta (GSK-3beta), the regulatory enzyme immediately upstream of GS, by serine
61 de strong evidence that NCED is indeed a key regulatory enzyme in ABA biosynthesis in leaves, and dem
62 Although it has never been reported as a regulatory enzyme in any system studied to date, kinetic
63 ene determining the activity of an important regulatory enzyme in catecholamine inactivation is assoc
64 of phosphoglucomutase 1 (PGM), an important regulatory enzyme in cellular glucose utilization and en
66 ivates acetyl-CoA carboxylase (ACC), the key regulatory enzyme in fatty acid biosynthesis, in the arc
67 er fructose-1,6-bisphosphatase (FBPase) is a regulatory enzyme in gluconeogenesis that is elevated by
74 cceptor) oxidoreductase, EC 1.7.99.5), a key regulatory enzyme in one-carbon metabolism, results in a
75 holine cytidylyltransferase (CCT) is the key regulatory enzyme in phosphatidylcholine (PC) synthesis
76 idermal ornithine decarboxylase (ODC), a key regulatory enzyme in polyamine biosynthesis, may suppres
77 hosphate dehydrogenase (IMPDH) is a critical regulatory enzyme in purine nucleotide biosynthesis that
78 cose (Glc) pyrophosphorylase (AGPase), a key regulatory enzyme in starch biosynthesis, is highly regu
86 latter group as purF, which encodes the key regulatory enzyme in the de novo purine synthetic pathwa
87 monophosphate dehydrogenase (IMPDH) is a key regulatory enzyme in the de novo synthesis of the purine
88 ic acid (ACC) synthase which is an important regulatory enzyme in the ethylene biosynthetic pathway.
91 a polypeptide revealed its identity as a key regulatory enzyme in the glycolytic pathway, namely phos
92 endent isocitrate dehydrogenase (IDH), a key regulatory enzyme in the Krebs cycle, is a multi-tetrame
93 ansferase (AANAT) is the penultimate and key regulatory enzyme in the melatonin biosynthetic pathway.
94 e to acetyl-CoA in mitochondria and is a key regulatory enzyme in the metabolism of glucose to acetyl
95 rnesyl pyrophosphate synthase (hFPPS), a key regulatory enzyme in the mevalonate pathway, catalyzes t
96 tors of IkappaB kinase-beta (IKKbeta), a key regulatory enzyme in the nuclear factor-kappaB (NF-kappa
98 e to acetyl-CoA in mitochondria and is a key regulatory enzyme in the oxidation of glucose to acetyl-
101 lutaryl coenzyme A (HMG-CoA) synthase, a key regulatory enzyme in the pathway for endogenous choleste
102 lutaryl-coenzyme A (HMG-CoA) synthase, a key regulatory enzyme in the pathway for endogenous choleste
103 din-endoperoxide synthase 2 (PTGS2) is a key regulatory enzyme in the synthesis of the antifibrotic a
104 (PDE) of retinal photoreceptors is a central regulatory enzyme in the visual transduction pathway of
105 e cytidylyltransferase (CCT) is an important regulatory enzyme in this pathway and that its activity
106 bifunctional substrate preference of the key regulatory enzyme in tocopherol (vitamin E) biosynthesis
109 stinct compartmentalization of PP2A and PP2A regulatory enzymes in plasma membrane microdomains and i
111 use the total amount of one of the principle regulatory enzymes in the extract (ACP, the enzyme compl
112 minant negative and dominant active forms of regulatory enzymes in the Ras/MAPK and PKB pathways and
113 apeutic potential of inhibiting two critical regulatory enzymes in this pathway-kynurenine-3-monooxyg
114 nfection stimulated expression of the immune regulatory enzyme indoleamine 2,3 dioxygenase (IDO) in l
115 is uniquely competent to express the T-cell regulatory enzyme indoleamine 2,3-dioxygenase (IDO) in m
116 brain, AKAP79/150 incorporates PKA and other regulatory enzymes into signal transduction networks tha
119 alterations in protein expression levels of regulatory enzymes involved in glucose and choline metab
120 erations in the protein expression levels of regulatory enzymes involved in lipid metabolism, includi
122 e previously shown declining activity of the regulatory enzyme lactosylceramide N-acetylglucosaminylt
124 affinity of receptors or in the activity of regulatory enzymes may alter the susceptibility of certa
125 -glucose pyrophosphorylase (AGPase) is a key regulatory enzyme of bacterial glycogen and plant starch
126 clopropane-1-carboxylic acid synthase, a key regulatory enzyme of ethylene biosynthesis) and LeIAA (A
127 encoding acetyl-CoA carboxylase-alpha, a key regulatory enzyme of fatty acid synthesis, is transcribe
128 e triphosphate citrate lyase (ACLY) is a key regulatory enzyme of glucose metabolism, cholesterol and
131 equences of elevated levels of Pfkfb3, a key regulatory enzyme of glycolysis, and found that pharmaco
137 ose-5-phosphate synthase (DXS), an important regulatory enzyme of the mevalonate-independent pathway
138 onine decarboxylase (AdoMetDC) is a critical regulatory enzyme of the polyamine biosynthetic pathway
141 In the yeast Saccharomyces cerevisiae, key regulatory enzymes of gluconeogenesis such as fructose-1
143 nd neutral sphingomyelinase (NSMase) are key regulatory enzymes of sphingolipid metabolism, promoting
144 oA reductase and acetyl-CoA carboxylase (key regulatory enzymes of sterol synthesis and fatty acid sy
146 ave demonstrated that flavonoids can inhibit regulatory enzymes or transcription factors important fo
148 Sirtuin enzymes and a substrate for multiple regulatory enzyme reactions within and outside the cell.
149 expression of the myofibrils and the calcium-regulatory enzyme SERCA2, and reduced the magnitude and
150 y showed that androgen induces the first and regulatory enzyme spermidine/spermine N1-acetyltransfera
151 es, which phosphorylate and thereby activate regulatory enzymes such as phospholipase C-gamma 1 and p
152 are reflected in the fractional states of a regulatory enzyme, such as the fraction of the total enz
153 teraction between these acylations and their regulatory enzymes, such as histone acetyltransferases,
154 rofiling to identify candidate substrates of regulatory enzymes, such as kinases and ubiquitin ligase
155 ne demethylase 5 (KDM5) family of epigenetic regulatory enzymes suppresses R-loop formation in genomi
156 nsferase (plsB) of Escherichia coli is a key regulatory enzyme that catalyzes the first committed ste
158 on in catechol-O-methyltransferase (COMT), a regulatory enzyme that controls dopamine availability.
162 merous functional aspects of a key metabolic regulatory enzyme that is important for high-titer viral
164 cible 6-phosphofructo-2-kinase, a glycolysis-regulatory enzyme that protects against diet-induced int
165 tosolic phospholipase A(2) (cPLA(2)alpha), a regulatory enzyme that releases arachidonic acid (AA) fo
166 ndoleamine 2,3-dioxygenase 1 (IDO1) is a key regulatory enzyme that supports Treg function and periph
167 clear accumulation of Nrf1 proteins, but the regulatory enzymes that act on Nrf1 are not fully define
170 ansferase subunit is a member of a family of regulatory enzymes that are known to control a range of
172 is a complex process involving a variety of regulatory enzymes that control the intracellular respon
173 and logic of the cell cycle, identified key regulatory enzymes that drive the cell cycle, elucidated
174 ons along with the transcription factors and regulatory enzymes that have been previously identified
177 increased by 40%) and the involvement of key regulatory enzymes, using isolated working rat hearts ex
178 hanism of tissue-specific expression of this regulatory enzyme, we characterized the major (type 2) C
179 1%; beta-HAD, 32%) and glycolytic (PFK, 18%) regulatory enzymes were also increased in mVEGF-/- mice.
180 redoxin reductases (TRs) are important redox regulatory enzymes, which control the redox state of thi
182 mic, effector-modified interactions of these regulatory enzymes with the flexibly held outer domains
184 choline cytidylyltransferase (CCT), the rate-regulatory enzyme within the CDP-choline pathway, by 40%