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共起表現

「KINASE」の共起表現一覧(1語右で並び替え)

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SLC9A3R2, as well as SLC9A3R1 and protein	kinase A phosphorylation, may play a role in NHE3 reg
ted inhibition of adenylyl cyclase and Protein	Kinase A Still, direct effects of CB1 receptors on me
is achieved by a similar mechanism, as protein	kinase A acts to phosphorylate the enzyme, which lowe
Downregulation of protein	kinase A occurs by a feedback mechanism: One of the s
The catalytic function of protein	kinase A would sometimes couple with the AKAP, bindin
myosin heavy chain	kinase A
ling molecules, including eIF3c, CD44, protein	kinase A and p21 activated kinases.
f binding to the regulatory subunit of protein	kinase A (PKA) and confining the holoenzyme to discre
Since the effects of protein	kinase A on the synthesis of proteins work by activat
astoma cells, it has been shown that a protein	kinase A (PKA) activator will increase the quantity o
H-89 is a Protein	kinase A inhibitor that also inhibits several other k
f cyclic-AMP and its downstream target protein	kinase A (PKA).
Protein	kinase A also has the ability to phosphorylate ACC, w
Protein	Kinase A, for example, can phosphorylate tryptophan h
te the phosphorylation of phosducin by protein	kinase A. The protein is thought to participate in th
ular cAMP and subsequent activation of protein	kinase A. This ultimately results in stimulation of s
Tyrosine-protein	kinase ABL2 also known as Abelson-related gene (Arg)
r names in common use include dihydroxyacetone	kinase, acetol kinase, and acetol kinase (phosphoryla
ll proliferation and mitogen-activated protein	kinase activation in microglia, but without producing
actor NHE-RF2 (NHERF-2) also known as tyrosine	kinase activator protein 1 (TKA-1) or SRY-interacting
lar transduction of receptor-mediated tyrosine	kinase activators.
on Ku to direct it to DNA ends and trigger its	kinase activity DNA-PKcs is required for the non-homo
Tyrosine	kinase activity mediates the GC-C signaling pathway w
The protein has	kinase activity and is thought to function in NMD by
Prostaglandin E2 activates HPK1	kinase activity via a PKA-dependent pathway.
The protein has serine/threonine	kinase activity and is a GTPase-activating protein fo
of hypoxic cancer cells through focal adhesion	kinase activity and cell-to-matrix adhesion.
Trx inhibits ASK1	kinase activity by direct binding to its N-terminal c
subunit of eukaryotic initiation factor 2. Its	kinase activity is induced by low levels of heme and
and stimulating the intrinsic protein-tyrosine	kinase activity of the receptor (see the second diagr
Sorivudine is phosphorylated by thymidine	kinase activity in the body and is absorbed into the
The tyrosine	kinase activity, in turn, initiates a signal transduc
PHA-665752 (Pfizer) specifically inhibits MET	kinase activity, and it has been demonstrated to repr
It has a third target: inhibiting RET-tyrosine	kinase activity, an important growth driver in certai
omerase II show significantly reduced Aurora B	kinase activity.
ation of ERKs leads to the activation of their	kinase activity.
f Raf-1 is associated with inhibition of Raf-1	kinase activity.
ther EGF receptor family members which do have	kinase activity.
STE20-related	kinase adapter protein beta is an enzyme that in huma
thin a virally infected cell a viral thymidine	kinase adds a phosphate group to the penciclovir mole
The serine-threonine protein	kinase AKT1 is catalytically inactive in serum-starve
dent manner by activating the serine/threonine	kinase AKT1, which then phosphorylates and inactivate
C-src tyrosine	kinase, also known as CSK, is a human protein and gen
In chemistry and biochemistry, a	kinase, alternatively known as a phosphotransferase,
ion of sphingosine is catalyzed by sphingosine	kinase, an enzyme ubiquitously found in the cytosol a
The receptors affect the downstream target AMP	kinase, an important cellular metabolic rate control
nscribing RNA, it stimulates T4 polynucleotide	kinase and T7 RNA polymerase activity, it binds to an
complex also contains 2 regulatory enzymes, a	kinase and a phosphorylase.
n vitro studies demonstrated that ERK, p38 MAP	kinase and Jun N-terminal kinase were all able to pho
quence of agonist stimulation of both tyrosine	kinase and G protein-coupled receptors.
me proteins such as the yeast phosphoglycerate	kinase and a mutant human ubiquitin, non-exponential
n which binds to the ATP binding pocket of the	kinase and modulates its function.
N-acetylglutamate	kinase, and
guanosine monophosphate	kinase, and
Other names in common use include type III PIP	kinase, and phosphatidylinositol 3-phosphate 5-kinase
names in common use include GALK2, GK2, GalNAc	kinase, and N-acetylgalactosamine (GalNAc)-1-phosphat
names in common use include inosine-guanosine	kinase, and inosine kinase (phosphorylating).
first added to a histidine residue within the	kinase, and later transferred to an aspartate residue
Stimulates T4 polynucleotide	kinase and T7 RNA polymerase activity
llular signalling pathways, especially protein	kinase and lipid kinase pathways.
, G-protein coupled receptor kinases, tyrosine	kinase, and cytomegalovirus pUL97 protein.
e presence of adenosine triphosphate, pyruvate	kinase, and phosphoenol pyruvate.
uclear factor κB and mitogen-activated protein	kinase and failed to induce downstream cytokines in r
Other names in common use include CTD	kinase, and STK9.
This	kinase and its regulatory subunit cyclin C are compon
osphorylating), L-rhamnulokinase, L-rhamnulose	kinase, and rhamnulose kinase.
inase activity, TG2 is proposed to also act as	kinase, and protein disulfide isomerase, and deamidas
boflavin (vitamin B2) by the enzyme riboflavin	kinase and functions as prosthetic group of various o
This gene encodes a member of the tyrosine	kinase and, more specifically, the Janus kinases (JAK
Serine/threonine-specific protein	kinase, as in bone morphogenetic protein
Receptor tyrosine	kinase, as in fibroblast growth factor receptor.
using 32P-labeled ATP, usually via an in vitro	kinase assay.
d make contact with the catalytic cleft of the	kinase at several key amino acids (usually through hy
In 1998, Aurora	kinase B was identified in humans by a polymerase cha
In the same year, rat Aurora	kinase B was identified in a screen designed to find
MAPK/ERK mitogenic pathway and the Akt/protein	kinase B (PKB) survival pathway.
Tyrosine-protein	kinase BAZ1B is an enzyme that in humans is encoded b
Other names in common use include	kinase, BCK, BCKD kinase, BCODH kinase, branched-chai
eptors is typically associated with a tyrosine	kinase belonging to the Janus kinase (JAK) family.
One difficulty is that the poxvirus thymidine	kinase belongs to the same family of thymidine kinase
Guanidinoacetate	kinase belongs to the family of transferases, specifi
stead associate with the TYRO protein tyrosine	kinase binding protein to transduce activating signal
This	kinase binds to TRAF2 and stimulates NF-κB activity.
The activation of this	kinase by tumor-necrosis factor alpha (TNF-alpha) is
MKK3 and SEK activate p38 MAP	kinase by phosphorylation at Thr180 and Tyr182, Activ
e is an observed irregular increase in protein	kinase C (PKC) activity within the brain.
Protein	kinase C delta type is an enzyme that in humans is en
unction in the absence of cAMP, ATP or protein	kinase C when in the presence of the activated α-subu
also been shown to be a substrate for protein	kinase C (PKC) phosphorylation.
ith other related compounds) acts as a protein	kinase C regulator, inducing localised inflammation t
The protein	kinase C (PKC) inhibitor Bis(indolyl)maleimide inhibi
DAG in turn is an inducer of protein	kinase C (PKC).
Modulation of protein synthesis and protein	Kinase C could be a mechanism.
potent, selective, and cell-permeable protein	kinase C inhibitor.
Protein	kinase C (PKC) is a family of serine- and threonine-s
has been shown to be via activation of protein	kinase C theta.
s to extracellular stimuli by inducing protein	kinase C and increasing cytosolic Ca(2+) concentratio
site, enzastaurin selectively inhibits protein	kinase C beta, an enzyme involved in the induction of
protein kinases, collectively known as protein	kinase C (PKC).
See also: Protein	kinase C
ide has been shown to activate various protein	kinase C (PKC) isoforms to cause the phosphorylation
It is a protein	kinase C inhibitor.
Protein	kinase C (PKC) is a family of serine- and threonine-s
Also activation of protein	kinase C decreased the current although in a non-reve
bisindolyl maleimide-based, nanomolar protein	kinase C inhibitors.
Protein	kinase C stimulates NHE3, while protein kinase A inhi
Protein	kinase C phosphorylation promotes localization of PCT
een the two copies of the C1 domain in Protein	Kinase C (that bind phorbol esters and diacylglycerol
The calphostins are inhibitors of protein	kinase C (PKC).
IP3 contributes to the activation of protein	kinase C (PKC).
signal transmission pathways, such as protein	kinase C and phospholipase C.
Safingol is a lyso-sphingolipid protein	kinase C inhibitor.
st detected, is the major substrate of protein	kinase C in platelets.
However, whether PKC (protein	kinase C) could activate MEK5 is not yet known.
Phorbol esters can directly stimulate protein	kinase C, PKC.
As an activator of protein	kinase C, it is a weak tumor promoter compared to 12-
Protein	kinase C-alpha (PKC-α) is a specific member of the pr
ating the receptor in a PKC-dependent (protein	kinase C-dependent) manner.
PKN3 is a protein	kinase C-related molecule and thought to be an effect
n and the central C1 domain similar to protein	kinase C. When lipid diacylglycerol (DAG) binds to th
gi and is dependent on the activity of protein	kinase C. Alpha-secretase activity in the golgi is th
It can inhibit protein	kinase C.
tumor promoters through activation of protein	kinase C.
y are regulated by Ca2+/calmodulin and protein	kinase C. In their unphosphorylated form, they bind t
nuclear DNA-dependent serine/threonine protein	kinase called DNA-PK.
The encoded protein is a general protein	kinase capable of phosphorylating several known prote
The MAP	kinase cascade can also be activated by certain heter
, of which the mitogen-activated protein (MAP)	kinase cascade has been well-studied.
RAF to MEK to MAPK is an example of a protein	kinase cascade.
Drugs that selectively down-regulate MAP	kinase cascades could prove to be valuable as therape
scription) and MAPK (mitogen activated protein	kinase) cascades.
The enzyme phosphoglycerate	kinase catalyses the phosphorylation of 3PGA by ATP (
DNA-dependent protein	kinase, catalytic subunit, also known as DNA-PKcs, is
amino acids (79.7 kilodaltons) with a protein	kinase catalytic domain that bears greatest sequence
forms a complex with the DNA-dependent protein	kinase catalytic subunit (DNA-PKcs) to form the full
Dolichol	kinase catalyzes CTP-mediated phosphorylation of doli
Lastly, adenylate	kinase catalyzes a reaction by which 2 ADP are combin
Triose	kinase catalyzes this step using ATP.
PITSLRE serine/threonine-protein	kinase CDC2L1 is an enzyme that in humans is encoded
PITSLRE serine/threonine-protein	kinase CDC2L2 is an enzyme that in humans is encoded
response activated ATM phosphorylates effector	kinase CHK2 which phophphorylates CDC25A, targeting i
is a catalytic subunit of the cyclin-dependent	kinase complex, whose activity is restricted to the G
MLCP activity is inhibited by Rhoa and Rho	kinase, components of the Ca2+ independent pathway fo
When Wnt is not present, GSK-3 (a	kinase) constitutively phosphorylates the β-catenin p
n did other enzymes tested (aldolase, pyruvate	kinase, creatine kinase, and lactate dehydrogenase).
Serine/threonine-protein	kinase DCLK1 is an enzyme that in humans is encoded b
Dolichol	kinase deficiency is a cutaneous condition caused by
Mevalonate	kinase deficiency has an autosomal recessive pattern
Pyruvate	kinase deficiency is the second most common cause of
d as an inborn error of metabolism, mevalonate	kinase deficiency usually results in developmental de
Mevalonate	kinase deficiency causes an accumulation of mevalonic
Mevalonate	kinase deficiency, also called mevalonic aciduria, is
er names in common use include deoxycytidylate	kinase, deoxycytidylate kinase, CMP kinase, CTP:CMP p
mmon use include deoxynucleoside monophosphate	kinase, deoxyribonucleoside monophosphokinase, and de
bitor blocks the ATP-binding site and puts the	kinase domain into an intermediate open conformation.
One of the active site residues in the protein	kinase domain of this protein is altered, and it is t
The N-terminal	kinase domain is able to phosphorylate histone H1.
Class III myosins, such as this one, have a	kinase domain N-terminal to the conserved N-terminal
	kinase domain (KD; PI3_PI4_kinase),
It encodes a protein with a tyrosine	kinase domain at the N-terminal end and a proline-ric
specific tyrosine residues within the tyrosine	kinase domain of each RET molecule.
ain of 39 to 129 residues in length, a protein	kinase domain and a short C-terminal domain containin
Where Thr-412 (activation loop of the	kinase domain) at PKCiota/lambda phosphorylates glyce
Without taking into account GAK's	kinase domain, GAK is 43% identical to auxilin, a neu
either transducing a signal through their own	kinase domain, or by initiating a signalling cascade
ermal growth factor receptor's (EGFR) tyrosine	kinase domain.
s an SH2 domain, an SH3 domain, and a tyrosine	kinase domain.
a neuregulin binding domain but not an active	kinase domain.
ne-spanning region, and a cytoplasmic tyrosine	kinase domain.
N-terminal LIM motifs and a C-terminal protein	kinase domain.
The alpha subunits have the catalytic	kinase domain.
FR5 lacks the classical activation loop in the	kinase domain.
involved in regulating the activity of the KD	kinase domain.
domain and in the C-terminal part the tyrosine	kinase domain.
ne-spanning segment and a cytoplasmic tyrosine	kinase domain.
nine residues and can discriminate between the	kinase domains of the EGFR and that of the insulin re
milarity of the proteins includes the tyrosine	kinase domains and extends amino-terminal to include
ropisomeric bisindolylmaleimides where the two	kinase domains, and two different inhibitor conformer
n associated PH domain, and 2 serine-threonine	kinase domains.
oded two isoforms of the human ser/thr protein	kinase EMK1.
The protein	kinase encoded by this gene could be cleaved by caspa
The IκB	kinase enzyme complex is part of the upstream NF-κB s
eIF-2 is a	kinase enzyme that phosphorylates eIF-2.
d thus no decomposition of cAMP which activate	kinase enzyme which phosphorylate hormone-sensitive l
tated that Tumor M2-PK, a form of the pyruvate	kinase enzyme, is produced in all rapidly-dividing ce
levels can be ruled out by measuring creatine	kinase enzymes.
Receptor tyrosine-protein	kinase erbB-3 is an enzyme that in humans is encoded
The WNK4 gene encodes a serine-threonine	kinase expressed in distal nephron.
this gene is a member of the cyclin-dependent	kinase family of Ser/Thr protein kinases.
ember of the serine/threonine-specific protein	kinase family related to NIMA (never in mitosis, gene
p34Cdc2	kinase family members are known to be essential for e
This gene encodes a member of the adenylate	kinase family of enzymes.
role for members of the proto-oncogene pp60src	kinase family in normal cell signalling.
ne is a member of the dual specificity protein	kinase family, which acts as a mitogen-activated prot
6 is a member of the dual specificity protein	kinase family, which functions as a mitogen-activated
s gene belongs to the serine/threonine protein	kinase family, and to the Ca(2+)/calmodulin-dependent
in encoded by this gene is a member of the MAP	kinase family.
s gene encodes a member of the Ser/Thr protein	kinase family.
s gene encodes a member of the p34Cdc2 protein	kinase family.
this gene is a member of the serine/threonine	kinase family.

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共起表現

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「KINASE」の共起表現一覧(1語右で並び替え)