「phosphorylation」の共起表現(2語右で並び替え)

Weblio 辞書 > 英和辞典・和英辞典 > phosphorylationの意味・解説 > phosphorylationに関連した共起表現

意味

例文

共起表現

「phosphorylation」の共起表現一覧(2語右で並び替え)

該当件数 : 198件

well-known for discovering that tyrosine	phosphorylation is a fundamental mechanism for transmembr
es because they catalyze auto- (or self-)	phosphorylation of a key conserved aspartate residue with
	Phosphorylation plays a key role in MAT function.
Upon	phosphorylation, Tir activates condensation and polymeriz
e reaction that leads to the recruitment,	phosphorylation, and activation of Type I activin recepto
the B cell receptors, Lyn undergoes rapid	phosphorylation and activation.
a caused by agents that inhibit oxidative	phosphorylation, early administration may improve outcome
on the energy-transfer system (oxidative	phosphorylation) and ADP binding sites of rat liver mitoc
The TCR cannot stimulate the	phosphorylation of Akt in that absence of p110δ activity.
kinase 3 (GSK-3) could be inhibited upon	phosphorylation by Akt, which results in promotion of gly
n extremely potent uncoupler of oxidative	phosphorylation with an IC50 of about 1 micromolar (≈500
r of the Medical Research Council Protein	Phosphorylation Unit, and a fellow of the Academia Europe
sponse to the state of the cell via their	phosphorylation state and again protect the message from
KinasePhos is a database describing some	phosphorylation networks associated with the information
r mechanism of Atg1 complex regulation by	phosphorylation of Atg13 through TOR kinase under nutrien
UCPs separate oxidative	phosphorylation from ATP synthesis with energy dissipated
Gjedde A (1982) Calculation of glucose	phosphorylation from brain uptake of glucose analogs in v
This reduces the need of oxidative	phosphorylation done by the TCA cycle via the electron tr
yotic initiation factor 2 from inhibitory	phosphorylation and by removing the amino-terminal methio
The	phosphorylation of c-Abl promotes actin polymerization.
ototropin protein will unfold and undergo	phosphorylation that can cause a cascade of events inside
	Phosphorylation of cardiac myosin heavy chains (see MYH7B
tem by uncoupling mitochondrial oxidative	phosphorylation, which causes a decrease in adenosine tri
Cdk activity can be reactivated after	phosphorylation by Cdc25.
	Phosphorylation of Cdc25C by CDS1 and CHK1 creates a bind
The tyrosine	phosphorylation of CDCP1 in cultured cells occurs when ce
The	phosphorylation of CDCP1 is seen in many cancers, includi
Cdr2 and Cdr1 inhibit Wee1, preventing	phosphorylation of Cdk1 and thereby leading to activation
Differential methylation and	phosphorylation of coilin likely influences its localizat
	Phosphorylation of ComA activates the expression of comS
y controlling focal adhesion kinase (FAK)	phosphorylation and cooperating with the α4β1 and α5β1 in
is required) to creatine (in liver), and	phosphorylation by creatine kinase (ATP is required) to p
The reversible	phosphorylation of creatine (i.e., both the forward and b
tein kinase C (PKC) isoforms to cause the	phosphorylation of Cx43, which aids in proper function of
This autophosphorylation leads to	phosphorylation of cytosolic targets as well as associati
it is able to bind reelin, leading to the	phosphorylation of DAB1, which binds on its cytosolic tai
rophic growth by glycolysis and oxidative	phosphorylation during dark periods.
The	PHOsphorylation SIte DAtabase PHOSIDA integrates thousand
he cytoplasm of the cell, often involving	phosphorylation or dephosphorylation of various other cyt
protein activation / inactivation (e.g.,	phosphorylation / dephosphorylation) across a set of prot
ospho3D is a database of 3D structures of	phosphorylation sites derived from Phospho.ELM.
By the	phosphorylation of diacylglycerol (DAG) by DAG kinase (DA
rocess is tightly regulated by reversible	phosphorylation of different phosphoinositides and their
This	phosphorylation provokes dissociation of ATM dimers, whic
l molecular weight inhibitors of tyrosine	phosphorylation, which do not inhibit protein kinases tha
Dolichol kinase catalyzes CTP-mediated	phosphorylation of dolichol, the terminal step in de novo
	Phosphorylation of E1 by pyruvate dehydrogenase kinase (P
Ultimately,	phosphorylation of Elk1 can result in the production of m
	Phosphorylation dramatically enhances the enzyme's capabi
substrate for dimerization and subsequent	phosphorylation by ERBB1, ERBB2 and ERBB4.
	Phosphorylation of ERKs leads to the activation of their
at mitochondria are the site of oxidative	phosphorylation in eukaryotes, which ushered in the moder
of ATP is available from substrate-level	phosphorylation, for example, in glycolysis.
Phospho.ELM is a database storing the	phosphorylation data extracted from the literature and th
TSC2 has 3	phosphorylation sites for RSK.
tree representatively, enables to examine	phosphorylation events from a global point of view includ
ysis metabolic pathway and is produced by	phosphorylation of fructose 6-phosphate.
o fructose 6-phosphate in preparation for	phosphorylation to Fructose-1,6-bisphosphate. The additio
cell, glucose 6-phosphate is produced by	phosphorylation of glucose on the sixth carbon.
and glucokinase; the latter catalyses the	phosphorylation of glucose to G6P and is not inhibited by
of cyclooxygenase-2 mRNA, and lead to the	phosphorylation of glycogen synthase kinase-3.
	Phosphorylation of glycogen synthase decreases its activi
Glycogen phosphorylase is activated by	phosphorylation, whereas glycogen synthase is inhibited.
Without this	phosphorylation, the glycoproteins are not destined for l
ation of MAPKAP kinase-2 and inhibits the	phosphorylation of heat shock protein 27.
Furthermore, cytokine-dependent GSK-3	phosphorylation in hemopoietic cells may regulate growth,
as PhosphoSitePlus, which details protein	phosphorylation in human, mouse and rat.
is protein is activated by signal-induced	phosphorylation; studies in rodents suggest that it is a
glycolysis, the Krebs cycle and oxidative	phosphorylation whereas in the absence of oxygen, water i
Importantly though, a third	phosphorylation site in the non-catalytic N terminus (the
This	phosphorylation results in the dissociation of IκBα from
It stimulates tyrosine	phosphorylation processes including the Jak2/STAT5 pathwa
or characterised by the amino acids whose	phosphorylation is inhibited: most kinases act on both se
It is necessary for cAMP-mediated	phosphorylation and inhibition of SLC9A3.
e kinase substrate that promotes tyrosine	phosphorylation of inositol 1,4,5-trisphosphate receptors
kines, arachidonate mobilization, protein	phosphorylation, and inositol phosphate formation.
In general,	phosphorylation destabilizes intermediate filaments.
sort cargo to the anterograde pathway the	phosphorylation pathway(s) involved in this phenomenon mi
cellular stores and promotes Lyn-mediated	phosphorylation of IP3 receptors 1 and 2.
PKC theta promotes serine	phosphorylation of IRS-1, thereby inhibiting the insulin
mab efficiently binds EGFR and blocks its	phosphorylation, it is not as effective as cetuximab (a c
either used as a substrate for oxidative	phosphorylation, or is converted to citrate for export to
The histidine	phosphorylation site is located at His-260.
ipates in transmembrane signaling through	phosphorylation of its intracellular domain.
vation of this receptor leads to tyrosine	phosphorylation of JAK1 and TYK2 kinases.
they mediate cell signals by inducing the	phosphorylation of key tyrosines, thus initiating the bin
they mediate cell signals by inducing the	phosphorylation of key tyrosines, thus initiating cell si
Zap70 - Binds to ITAM sequences upon	phosphorylation by Lck and Fyn
Their ITIM	phosphorylation subsequently leads to recruitment and act
ile side chains and modifications such as	phosphorylation are left intact.
Protein kinase C	phosphorylation promotes localization of PCTP to the mito
Also, the	phosphorylation of M-Cdk (a complex of Cdk1 and cyclin B)
nes, this kinase is activated through its	phosphorylation by MAP kinases including MAPK1/ERK, MAPK1
cussed below, many additional targets for	phosphorylation by MAPK were later found, and the protein
In addition,	phosphorylation by MAPK, PKA, PKC or cdc2 alters the acti
tabolic H217O water produced by oxidative	phosphorylation in mitochondria).
ic and acts by interfering with oxidative	phosphorylation in mitochondria, causing depletion of ATP
substance containing phosphoric acid (see	phosphorylation for more).
enerative diseases which exhibit abnormal	phosphorylation of neuronal cytoskeletal proteins by p25/
eotide (NAD)+ and are highly specific for	phosphorylation of nicotinamide riboside.
ins on the cytoplasmic face of SERCA: the	phosphorylation and nucleotide-binding domains, which for
Decreased Erk-mediated Elk1	phosphorylation is observed in the hippocampus and prefro
Similar	phosphorylation events occur in DAT and NET, decreasing t
involves the effects of bile acids on the	phosphorylation mechanism of the PKC family of proteins.
Similarly, length variations in the CK1ε	phosphorylation site of PER3 have been found to correlate
with tyrosine kinases, PTPs regulate the	phosphorylation state of many important signalling molecu
Mutations and variants of the CK1ε	phosphorylation site of PER2 are associated with cases of
The two main	phosphorylation sites on Lck are tyrosines 394 and 505.
gulation as there are many other possible	phosphorylation sites on ACC.
ssed in human epithelial tissues, but its	phosphorylation is only seen in mitotically detached or s
city of modification by processes such as	phosphorylation, methylation, or glycosylation.
tyrphostins, the short name for “tyrosine	phosphorylation inhibitor”, originally coined in a 1988 p
tion of ATP by the usual means, oxidative	phosphorylation or other energy-producing pathways such a
transcription, for example, by leading to	phosphorylation of other transcription factors.
The process appears to be regulated by	phosphorylation and oxygenation.
This kinase is regulated through direct	phosphorylation by p38 MAP kinase.
regulate various biological functions by	phosphorylation of particular target molecules (such as t
in cyclic nucleotide levels modulate the	phosphorylation of phosducin by protein kinase A. The pro
ducts obtained by cleavage of PIP3, or by	phosphorylation of PI(3)P, PI(4)P or PI(5)P.
argeting of substrates to be regulated by	phosphorylation (by PKA) and dephosphorylation (by phosph
	Phosphorylation takes place at the α-subunit which is a t
as well as SLC9A3R1 and protein kinase A	phosphorylation, may play a role in NHE3 regulation.
It also uncouples oxidative	phosphorylation, the process cells use to synthesize Aden
Upon	phosphorylation, this protein recruits multiple adaptor p
iffuse throughout the cytoplasm, but upon	phosphorylation, the protein begins to target certain are
CA is normally inhibited by the defective	phosphorylation of protein phospholamban, with which it i
Regulated by	phosphorylation and proteolysis.
of receptor desensitization via receptor	phosphorylation, beta-arrestin recruitment, and receptor
is found to undergo cell cycle-dependent	phosphorylation, which regulates its nuclear matrix and c
"Dinitrophenol uncouples oxidative	phosphorylation, causes release of calcium from mitochond
RhoA-mediated contractility and tyrosine	phosphorylation in response to adhesion.
ATF-2	phosphorylation in response to treatment of cells with tu
	Phosphorylation can result when the hormones glucagon or
es as an instructive example that protein	phosphorylation may result in both activation and inhibit
he Calvin Cycle, RuBP is a product of the	phosphorylation of ribulose-5-phosphate by ATP.
This event stimulates the subsequent	phosphorylation of S6K1 by PDK1.
The RS domain is subject to serine	phosphorylation, which seems to control interactions with
Post-translational modifications, such as	Phosphorylation or sequestration) or by means of irrevers
	Phosphorylation of Ser/Thr-Pro motifs in substrates is re
Postranslational modifications such as	phosphorylation on Ser16 inhibit the ability of Pin1 to b
Regulation of translation initiation via	phosphorylation of Ser51 in eIF2's α-subunit.
The	phosphorylation of serine 518 is known to alter the funct
role in increasing the rate of oxidative	phosphorylation in skeletal muscle.
gands to extracellular receptors triggers	phosphorylation of Smad2 at a Serine-Serine-Methionine-Se
It has been suggested that	phosphorylation of Smoothened plays a role in Hh-dependen
proteins may be involved with anchoring,	phosphorylation or some other modulatory or support funct
RNA interference and protein	phosphorylation in space environment using the nematode C
	Phosphorylation of sphingosine is catalyzed by sphingosin
ase (SPHK), the enzyme that catalyzes the	phosphorylation of sphingosine.
ranscription (STAT) pathway, resulting in	phosphorylation of STAT6.
d dependence on the rate limiting step of	phosphorylation of stavudine to stavudine monophosphate.
nded, as it can inhibit the intracellular	phosphorylation of stavudine.
tes, hinting its potential regulation via	phosphorylation, a step of the ceramide metabolism that c
ons may be N- or O- linked glycosylation,	phosphorylation, tyrosin sulfation or other.
It also inhibits the	phosphorylation of tau protein induced by Cdk5/p25 expres
smic tail containing a potential tyrosine	phosphorylation site that may bind SH2.
the cysteine group which is required for	phosphorylation; however the tension-like N terminal subd
tivated JAK kinases, and are activated by	phosphorylation of the Stat1.
These are all responsible for the	phosphorylation of the alpha subunit of eIF-2 at serine 5
AFPep also inhibits	phosphorylation of the estrogen receptor and activates th
ylcholine receptor aggregation as well as	phosphorylation of the MuSK receptor, they spliced them a
The protein was found to undergo	phosphorylation in the host cell.
. and Ferrell, J. E. Jr. (2002) Multisite	Phosphorylation and the Countdown to S Phase.
The nerve secretes agrin, resulting in	phosphorylation of the MuSK receptor.
e kinase) is an enzyme that catalyzes the	phosphorylation of the amino acid aspartate.
Chemiosmotic	phosphorylation is the third pathway that produces ATP fr
n Nature, niclosamide uncouples oxidative	phosphorylation in the tapeworm.
Deletion of the C-terminus of CNP or	phosphorylation abolish the catalytic activity of microtu
ttack and destroy acetylcholinesterase by	phosphorylation, so the action of acetylcholine becomes p
Differences in expression, sequence and	phosphorylation among the various fimbrin isoforms sugges
The	phosphorylation induces the dissociation of this protein
	Phosphorylation is the transfer of a phosphate group to a
C-terminus of Snf3 which facilitates the	phosphorylation of the two proteins by YckI.
One major example of this is	phosphorylation of the Ser-571 residue by glycogen syntha
ity also results in the activation of the	phosphorylation of the ezrin-moesin-radixin group promoti
negative regulatory domain at two sites;	phosphorylation at these sites appears to stimulate mTOR
ditional regulation is provided by Ser16;	phosphorylation of this residue does not alter enzyme con
MKK3 and SEK activate p38 MAP kinase by	phosphorylation at Thr180 and Tyr182, Activated p38 MAP k
The tyrosine	phosphorylation of Trask is tightly regulated and recipro
Metabolic studies showed more efficient	phosphorylation to triphosphate active form
K252a inhibits tyrosine	phosphorylation of Trk A induced by NGF.
The functional implications of CDCP1	phosphorylation in tumors is currently under investigatio
This protein is activated through	phosphorylation of two residues, tyrosine 705 and serine
omplex after ligand binding, resulting in	phosphorylation of type I receptors by type II receptors.
lthough membrane ion channels and protein	phosphorylation are typically indirectly affected by G pr
	Phosphorylation of Tyr905 stabilizes the active conformat
Cortactin is activated via	phosphorylation, by tyrosine kinases or serine/threonine
ransmission of inhibitory signals through	phosphorylation of tyrosine residues within the immunorec
scade of signaling events mediated by Lyn	phosphorylation of tyrosine residues within the immunorec
l mechanism of ATP synthesis by oxidative	phosphorylation was unknown.
ck inhibitory mechanisms that involve the	phosphorylation of upstream kinases.
he activation of this kinase requires its	phosphorylation by upstream kinases.
The consequence of GSK-3	phosphorylation is usually inhibition of the substrate.
PKCD is also regulated by	phosphorylation on various tyrosine residues including Y3
of signal transduction cascades (through	phosphorylation of various proteins).
It is known that Abi1 enhances the	phosphorylation of WAVE2 by c-Abl.
In addition, reduced	phosphorylation potential within hepatocytes can occur wi
rance develops, including opioid receptor	phosphorylation (which would change the receptor conforma

共起表現

「phosphorylation」の共起表現(2語右で並び替え) - Weblio英語共起表現検索

「phosphorylation」の共起表現一覧(2語右で並び替え)