「Phosphorylation」の共起表現(1語右で並び替え)

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共起表現

「Phosphorylation」の共起表現一覧(1語右で並び替え)

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tes, hinting its potential regulation via	phosphorylation, a step of the ceramide metabolism that c
Deletion of the C-terminus of CNP or	phosphorylation abolish the catalytic activity of microtu
Differences in expression, sequence and	phosphorylation among the various fimbrin isoforms sugges
on the energy-transfer system (oxidative	phosphorylation) and ADP binding sites of rat liver mitoc
ins on the cytoplasmic face of SERCA: the	phosphorylation and nucleotide-binding domains, which for
Regulated by	phosphorylation and proteolysis.
The process appears to be regulated by	phosphorylation and oxygenation.
. and Ferrell, J. E. Jr. (2002) Multisite	Phosphorylation and the Countdown to S Phase.
the B cell receptors, Lyn undergoes rapid	phosphorylation and activation.
It is necessary for cAMP-mediated	phosphorylation and inhibition of SLC9A3.
kines, arachidonate mobilization, protein	phosphorylation, and inositol phosphate formation.
e reaction that leads to the recruitment,	phosphorylation, and activation of Type I activin recepto
yotic initiation factor 2 from inhibitory	phosphorylation and by removing the amino-terminal methio
y controlling focal adhesion kinase (FAK)	phosphorylation and cooperating with the α4β1 and α5β1 in
lthough membrane ion channels and protein	phosphorylation are typically indirectly affected by G pr
ile side chains and modifications such as	phosphorylation are left intact.
MKK3 and SEK activate p38 MAP kinase by	phosphorylation at Thr180 and Tyr182, Activated p38 MAP k
negative regulatory domain at two sites;	phosphorylation at these sites appears to stimulate mTOR
of receptor desensitization via receptor	phosphorylation, beta-arrestin recruitment, and receptor
Cortactin is activated via	phosphorylation, by tyrosine kinases or serine/threonine
is required) to creatine (in liver), and	phosphorylation by creatine kinase (ATP is required) to p
Cdk activity can be reactivated after	phosphorylation by Cdc25.
he activation of this kinase requires its	phosphorylation by upstream kinases.
This kinase is regulated through direct	phosphorylation by p38 MAP kinase.
Zap70 - Binds to ITAM sequences upon	phosphorylation by Lck and Fyn
In addition,	phosphorylation by MAPK, PKA, PKC or cdc2 alters the acti
kinase 3 (GSK-3) could be inhibited upon	phosphorylation by Akt, which results in promotion of gly
substrate for dimerization and subsequent	phosphorylation by ERBB1, ERBB2 and ERBB4.
cussed below, many additional targets for	phosphorylation by MAPK were later found, and the protein
nes, this kinase is activated through its	phosphorylation by MAP kinases including MAPK1/ERK, MAPK1
	Phosphorylation can result when the hormones glucagon or
"Dinitrophenol uncouples oxidative	phosphorylation, causes release of calcium from mitochond
Phospho.ELM is a database storing the	phosphorylation data extracted from the literature and th
In general,	phosphorylation destabilizes intermediate filaments.
This reduces the need of oxidative	phosphorylation done by the TCA cycle via the electron tr
	Phosphorylation dramatically enhances the enzyme's capabi
rophic growth by glycolysis and oxidative	phosphorylation during dark periods.
a caused by agents that inhibit oxidative	phosphorylation, early administration may improve outcome
tree representatively, enables to examine	phosphorylation events from a global point of view includ
Similar	phosphorylation events occur in DAT and NET, decreasing t
ts on cardiomyocyte gap junctions through	phosphorylation events.
SC2 is not remarkably influenced by these	phosphorylation events.
of ATP is available from substrate-level	phosphorylation, for example, in glycolysis.
substance containing phosphoric acid (see	phosphorylation for more).
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
the cysteine group which is required for	phosphorylation; however the tension-like N terminal subd
RhoA-mediated contractility and tyrosine	phosphorylation in response to adhesion.
tabolic H217O water produced by oxidative	phosphorylation in mitochondria).
Furthermore, cytokine-dependent GSK-3	phosphorylation in hemopoietic cells may regulate growth,
The protein was found to undergo	phosphorylation in the host cell.
ATF-2	phosphorylation in response to treatment of cells with tu
RNA interference and protein	phosphorylation in space environment using the nematode C
The functional implications of CDCP1	phosphorylation in tumors is currently under investigatio
n Nature, niclosamide uncouples oxidative	phosphorylation in the tapeworm.
ic and acts by interfering with oxidative	phosphorylation in mitochondria, causing depletion of ATP
as PhosphoSitePlus, which details protein	phosphorylation in human, mouse and rat.
role in increasing the rate of oxidative	phosphorylation in skeletal muscle.
at mitochondria are the site of oxidative	phosphorylation in eukaryotes, which ushered in the moder
The	phosphorylation induces the dissociation of this protein
first to develop systematically tyrosine	phosphorylation inhibitors (tyrphostins) against a wide s
tyrphostins, the short name for “tyrosine	phosphorylation inhibitor”, originally coined in a 1988 p
well-known for discovering that tyrosine	phosphorylation is a fundamental mechanism for transmembr
or characterised by the amino acids whose	phosphorylation is inhibited: most kinases act on both se
ssed in human epithelial tissues, but its	phosphorylation is only seen in mitotically detached or s
Chemiosmotic	phosphorylation is the third pathway that produces ATP fr
The consequence of GSK-3	phosphorylation is usually inhibition of the substrate.
	Phosphorylation is the transfer of a phosphate group to a
Decreased Erk-mediated Elk1	phosphorylation is observed in the hippocampus and prefro
mab efficiently binds EGFR and blocks its	phosphorylation, it is not as effective as cetuximab (a c
es as an instructive example that protein	phosphorylation may result in both activation and inhibit
as well as SLC9A3R1 and protein kinase A	phosphorylation, may play a role in NHE3 regulation.
involves the effects of bile acids on the	phosphorylation mechanism of the PKC family of proteins.
city of modification by processes such as	phosphorylation, methylation, or glycosylation.
KinasePhos is a database describing some	phosphorylation networks associated with the information
ase (SPHK), the enzyme that catalyzes the	phosphorylation of sphingosine.
e kinase substrate that promotes tyrosine	phosphorylation of inositol 1,4,5-trisphosphate receptors
in cyclic nucleotide levels modulate the	phosphorylation of phosducin by protein kinase A. The pro
ck inhibitory mechanisms that involve the	phosphorylation of upstream kinases.
ipates in transmembrane signaling through	phosphorylation of its intracellular domain.
	Phosphorylation of cardiac myosin heavy chains (see MYH7B
ransmission of inhibitory signals through	phosphorylation of tyrosine residues within the immunorec
es because they catalyze auto- (or self-)	phosphorylation of a key conserved aspartate residue with
of cyclooxygenase-2 mRNA, and lead to the	phosphorylation of glycogen synthase kinase-3.
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
ducts obtained by cleavage of PIP3, or by	phosphorylation of PI(3)P, PI(4)P or PI(5)P.
	Phosphorylation of Tyr905 stabilizes the active conformat
	Phosphorylation of ComA activates the expression of comS
This protein is activated through	phosphorylation of two residues, tyrosine 705 and serine
regulate various biological functions by	phosphorylation of particular target molecules (such as t
they mediate cell signals by inducing the	phosphorylation of key tyrosines, thus initiating the bin
scade of signaling events mediated by Lyn	phosphorylation of tyrosine residues within the immunorec
	Phosphorylation of glycogen synthase decreases its activi
AFPep also inhibits	phosphorylation of the estrogen receptor and activates th
By the	phosphorylation of diacylglycerol (DAG) by DAG kinase (DA
K252a inhibits tyrosine	phosphorylation of Trk A induced by NGF.
The	phosphorylation of c-Abl promotes actin polymerization.
This event stimulates the subsequent	phosphorylation of S6K1 by PDK1.
ylcholine receptor aggregation as well as	phosphorylation of the MuSK receptor, they spliced them a
	Phosphorylation of Ser/Thr-Pro motifs in substrates is re
	Phosphorylation of E1 by pyruvate dehydrogenase kinase (P
vation of this receptor leads to tyrosine	phosphorylation of JAK1 and TYK2 kinases.
PKC theta promotes serine	phosphorylation of IRS-1, thereby inhibiting the insulin
he Calvin Cycle, RuBP is a product of the	phosphorylation of ribulose-5-phosphate by ATP.
The TCR cannot stimulate the	phosphorylation of Akt in that absence of p110δ activity.
Also, the	phosphorylation of M-Cdk (a complex of Cdk1 and cyclin B)
cell, glucose 6-phosphate is produced by	phosphorylation of glucose on the sixth carbon.
ysis metabolic pathway and is produced by	phosphorylation of fructose 6-phosphate.
It also inhibits the	phosphorylation of tau protein induced by Cdk5/p25 expres
It is known that Abi1 enhances the	phosphorylation of WAVE2 by c-Abl.
Regulation of translation initiation via	phosphorylation of Ser51 in eIF2's α-subunit.
ation of MAPKAP kinase-2 and inhibits the	phosphorylation of heat shock protein 27.
The nerve secretes agrin, resulting in	phosphorylation of the MuSK receptor.
	Phosphorylation of ERKs leads to the activation of their
nded, as it can inhibit the intracellular	phosphorylation of stavudine.
e kinase) is an enzyme that catalyzes the	phosphorylation of the amino acid aspartate.
The	phosphorylation of serine 518 is known to alter the funct
Cdr2 and Cdr1 inhibit Wee1, preventing	phosphorylation of Cdk1 and thereby leading to activation
It has been suggested that	phosphorylation of Smoothened plays a role in Hh-dependen
r mechanism of Atg1 complex regulation by	phosphorylation of Atg13 through TOR kinase under nutrien
yme phosphoglycerate kinase catalyses the	phosphorylation of 3PGA by ATP (which was produced in the
omplex acts to substantially increase the	phosphorylation of β-catenin by facilitating the action o
Dolichol kinase catalyzes CTP-mediated	phosphorylation of dolichol, the terminal step in de novo
CA is normally inhibited by the defective	phosphorylation of protein phospholamban, with which it i
The tyrosine	phosphorylation of Trask is tightly regulated and recipro
The reversible	phosphorylation of creatine (i.e., both the forward and b
rocess is tightly regulated by reversible	phosphorylation of different phosphoinositides and their
	Phosphorylation of Cdc25C by CDS1 and CHK1 creates a bind
cellular stores and promotes Lyn-mediated	phosphorylation of IP3 receptors 1 and 2.
Differential methylation and	phosphorylation of coilin likely influences its localizat
ditional regulation is provided by Ser16;	phosphorylation of this residue does not alter enzyme con
	Phosphorylation of sphingosine is catalyzed by sphingosin
eotide (NAD)+ and are highly specific for	phosphorylation of nicotinamide riboside.
it is able to bind reelin, leading to the	phosphorylation of DAB1, which binds on its cytosolic tai
transcription, for example, by leading to	phosphorylation of other transcription factors.
omplex after ligand binding, resulting in	phosphorylation of type I receptors by type II receptors.
they mediate cell signals by inducing the	phosphorylation of key tyrosines, thus initiating cell si
of signal transduction cascades (through	phosphorylation of various proteins).
enerative diseases which exhibit abnormal	phosphorylation of neuronal cytoskeletal proteins by p25/
tein kinase C (PKC) isoforms to cause the	phosphorylation of Cx43, which aids in proper function of
C-terminus of Snf3 which facilitates the	phosphorylation of the two proteins by YckI.
okinase is an enzyme that facilitates the	phosphorylation of α-D-galactose to galactose 1-phosphate
and glucokinase; the latter catalyses the	phosphorylation of glucose to G6P and is not inhibited by
One major example of this is	phosphorylation of the Ser-571 residue by glycogen syntha
d dependence on the rate limiting step of	phosphorylation of stavudine to stavudine monophosphate.
gands to extracellular receptors triggers	phosphorylation of Smad2 at a Serine-Serine-Methionine-Se
Ultimately,	phosphorylation of Elk1 can result in the production of m
The tyrosine	phosphorylation of CDCP1 in cultured cells occurs when ce
The	phosphorylation of CDCP1 is seen in many cancers, includi
ity also results in the activation of the	phosphorylation of the ezrin-moesin-radixin group promoti
This autophosphorylation leads to	phosphorylation of cytosolic targets as well as associati
ranscription (STAT) pathway, resulting in	phosphorylation of STAT6.
PKCD is also regulated by	phosphorylation on various tyrosine residues including Y3
Postranslational modifications such as	phosphorylation on Ser16 inhibit the ability of Pin1 to b
tion of ATP by the usual means, oxidative	phosphorylation or other energy-producing pathways such a
he cytoplasm of the cell, often involving	phosphorylation or dephosphorylation of various other cyt
either used as a substrate for oxidative	phosphorylation, or is converted to citrate for export to
proteins may be involved with anchoring,	phosphorylation or some other modulatory or support funct
Post-translational modifications, such as	Phosphorylation or sequestration) or by means of irrevers
sort cargo to the anterograde pathway the	phosphorylation pathway(s) involved in this phenomenon mi
	Phosphorylation plays a key role in MAT function.
In addition, reduced	phosphorylation potential within hepatocytes can occur wi
It stimulates tyrosine	phosphorylation processes including the Jak2/STAT5 pathwa
Protein kinase C	phosphorylation promotes localization of PCTP to the mito
This	phosphorylation provokes dissociation of ATM dimers, whic
This	phosphorylation results in the dissociation of IκBα from
smic tail containing a potential tyrosine	phosphorylation site that may bind SH2.
Similarly, length variations in the CK1ε	phosphorylation site of PER3 have been found to correlate
Importantly though, a third	phosphorylation site in the non-catalytic N terminus (the
The histidine	phosphorylation site is located at His-260.
The	PHOsphorylation SIte DAtabase PHOSIDA integrates thousand
Mutations and variants of the CK1ε	phosphorylation site of PER2 are associated with cases of
TSC2 has 3	phosphorylation sites for RSK.
ospho3D is a database of 3D structures of	phosphorylation sites derived from Phospho.ELM.
The two main	phosphorylation sites on Lck are tyrosines 394 and 505.
gulation as there are many other possible	phosphorylation sites on ACC.
ttack and destroy acetylcholinesterase by	phosphorylation, so the action of acetylcholine becomes p
with tyrosine kinases, PTPs regulate the	phosphorylation state of many important signalling molecu
sponse to the state of the cell via their	phosphorylation state and again protect the message from
also act as a repressor, dependent on its	phosphorylation state.
is protein is activated by signal-induced	phosphorylation; studies in rodents suggest that it is a
Their ITIM	phosphorylation subsequently leads to recruitment and act
	Phosphorylation takes place at the α-subunit which is a t
ototropin protein will unfold and undergo	phosphorylation that can cause a cascade of events inside
Without this	phosphorylation, the glycoproteins are not destined for l
iffuse throughout the cytoplasm, but upon	phosphorylation, the protein begins to target certain are
It also uncouples oxidative	phosphorylation, the process cells use to synthesize Aden
Upon	phosphorylation, this protein recruits multiple adaptor p
Upon	phosphorylation, Tir activates condensation and polymeriz
o fructose 6-phosphate in preparation for	phosphorylation to Fructose-1,6-bisphosphate. The additio
Metabolic studies showed more efficient	phosphorylation to triphosphate active form
ons may be N- or O- linked glycosylation,	phosphorylation, tyrosin sulfation or other.
r of the Medical Research Council Protein	Phosphorylation Unit, and a fellow of the Academia Europe
l mechanism of ATP synthesis by oxidative	phosphorylation was unknown.
glycolysis, the Krebs cycle and oxidative	phosphorylation whereas in the absence of oxygen, water i
Glycogen phosphorylase is activated by	phosphorylation, whereas glycogen synthase is inhibited.
is found to undergo cell cycle-dependent	phosphorylation, which regulates its nuclear matrix and c
l molecular weight inhibitors of tyrosine	phosphorylation, which do not inhibit protein kinases tha
The RS domain is subject to serine	phosphorylation, which seems to control interactions with

1 2 次へ＞

共起表現

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「Phosphorylation」の共起表現一覧(1語右で並び替え)