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miR (show MYLIP Proteins)-375 directly targeted PDK1 (show PDK1 Proteins) in porcine pancreatic stem cells suppressing cell proliferation and differentiation into islet-like cells.
Together these results indicate a strong potential regulatory role for PDK1 (show PDK1 Proteins) in OC stimulatory pathways (Akt (show AKT1 Proteins), ERK (show EPHB2 Proteins)) and autophagy induction (via mTORC1), which may contribute to the OC phenotype in Paget's disease of bone.
It targeted the 3-phosphoinositide-dependent protein kinase 1 gene that appeared to be a potent regulator of AKT (show AKT1 Proteins).
High (show PDK1 Proteins)ly expressed PDK1 could promote cell invasion and secretion of IL-1beta and IL-6 in human rheumatoid arthritis s (show PDK1 Proteins)ynovial (show PDK1 Proteins)MH7A c (show RPS6KA3 Proteins)ells. Inhib (show RPS6KA3 Proteins)ition of RSK2 reduced the PDK (show ASF1A Proteins)1-induced cell invasion and cytokines secretion (show PDK1 Proteins) in M (show RPS6KA3 Proteins)H7A cells. In response to TNF-alpha, PDK1 could phosphorylate RSK2 and activated RSK2, then promoting the activation of NF-kappaB.
In cancer cells resistant to PI3Kalpha inhibition, PDK1 blockade restores sensitivity to these therapies. SGK1, which is activated by PDK1, contributes to the maintenance of residual mTORC1 activity through direct phosphorylation and inhibition of TSC2.
Results suggest that Ser (show SIGLEC1 Proteins)-64 is an important phosphorylation site that is part of a positive feedback loop for human PDK1 (show PDK1 Proteins)-PKCtheta (show PRKCQ Proteins);-mediated T cell activation.
Elevated expression of PDK1 (show PDK1 Proteins) was an independent negative prognostic factor of gastric carcinoma.
miR (show MLXIP Proteins)-138-1* played a critical role in aflatoxin B1-induced malignant transformation of B-2A13 cells by targeting PDK1 (show PDK1 Proteins).
miR (show MLXIP Proteins)-454 functions as a tumor suppressor in glioblastoma, inhibiting proliferation of human glioblastoma cells by suppressing PDK1 (show PDK1 Proteins) expression.
Decreased PDK1 (show PDK1 Proteins) level is closely associated with reduced Akt (show AKT1 Proteins)/cyclin D1 (show CCND1 Proteins) activity.
MiR (show MLXIP Proteins)-138 regulation of PI3K (show PIK3CA Proteins) signaling in ASMCs by altering the expression of PDK1 (show PDK1 Proteins).
PDK1 signaling regulates the basal-to-suprabasal switch in developing epidermis by acting as both an activator and organizer of asymmetric cell division and the Notch (show NOTCH1 Proteins)-dependent differentiation program.
Data indicate that mammary-specific ablation of 3-phosphoinositide dependent protein kinase 1 (PDK1) could delay tumor initiation, progression and metastasis in a spontaneous mouse tumor model.
PDK1 was highly expressed in synovia of collagen-induced-arthritis mice compared to control. The expressions of PDK1, p-PDK1, RSK2 (show RPS6KA3 Proteins) and p-RSK2 (show RPS6KA3 Proteins) were all up-regulated in CIA (show NCOA5 Proteins) compared with normal. This indicated that PDK1/RSK2 (show RPS6KA3 Proteins) may participate in inflammatory progress of RA.
PDK1 is required for Ca(2 (show CA2 Proteins)+)-dependent platelet activation on stimulation of collagen receptor (show ITGA2 Proteins) glycoprotein VI, arterial thrombotic occlusion, and ischemic stroke in vivo.
In conclusion, we have identified that ARL15 acts as an insulin (show INS Proteins)-sensitizing effector molecule to upregulate the phosphorylation of members of the canonical IR/IRS1 (show IRS1 Proteins)/PDPK1/AKT (show AKT1 Proteins) insulin (show INS Proteins) pathway by interacting with its GAP ASAP2 (show ASAP2 Proteins) and activating PDPK1. This research may provide new insights into GTPase (show RACGAP1 Proteins)-mediated insulin (show INS Proteins) signalling regulation and facilitate the development of new pharmacotherapeutic targets for insulin (show INS Proteins) sensitizati
Only when suboptimal doses of Akt (show AKT1 Proteins)-Pdpk1 interaction inhibitor NSC156529 were used an additive effect with Notch (show NOTCH1 Proteins) inhibition was seen. We conclude that the Akt (show AKT1 Proteins) pathway inhibitor NSC156529 is potentially useful as single treatment for liver tumors with hyperactivated Akt (show AKT1 Proteins) signaling.
Xanthium strumarium methanolic extract exerts anti-inflammatory activity in vitro and in vivo by inhibiting PDK1 kinase activity and blocking signaling to its downstream transcription factor, NF-kappaB (show NFKB1 Proteins).
PDPK1 is required for exercise-induced cardiac hypertrophy but does not contribute to exercise-induced increases in mitochondrial function.
The PDK1 knock-in mice displayed a reduced brain size due to a reduction in neuronal cell size rather than cell number.
PDK1 is an important regulator in arterial thrombosis formation.
The authors show that loss of frataxin homolog (fh (show FXN Proteins)) in Drosophila leads to iron toxicity, which in turn induces sphingolipid synthesis and ectopically activates 3-phosphoinositide dependent protein kinase-1 (Pdk1) and myocyte enhancer factor-2 (Mef2 (show MYEF2 Proteins)).
PDK1 is also a presynaptic protein, though it is distributed more broadly.
dS6K activity is dependent on the Drosophila homologue of the phosphoinositide-dependent protein kinase (show CDK7 Proteins) 1, dPDK1
at least three C. elegans MTMs play essential roles in coelomocyte endocytosis, a process that also requires VPS34 (show PIK3C3 Proteins) (PI3K)
Piriformospora indica-stimulated growth response is mediated by a pathway consisting of the PLD-PDK1-OXI1 cascade.
PDK1 (show PDK1 Proteins) undergoes autophosphorylation at several sites; mutation of Ser (show SIGLEC1 Proteins)-276 to Ala resulted in enzyme with no detectable autophosphorylation; other sites important for autophosphorylation &/or activity were Asp (show ASIP Proteins)-167, Thr (show TRH Proteins)-176, & Thr (show TRH Proteins)-211
PDK1 (show PDK1 Proteins) is a potent enhancer of PID (show MTA2 Proteins) activity.
specific lipid signaling pathways converge on PTI1-2 via the PDK1-OXI1 axis
This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and single representatives of the gamma, delta, and epsilon subunits. The proton channel likely has nine subunits (a, b, c, d, e, f, g, F6 and 8). There are three separate genes which encode subunit c of the proton channel and they specify precursors with different import sequences but identical mature proteins. The protein encoded by this gene is one of three precursors of subunit c. Alternatively spliced transcript variants encoding different isoforms have been identified. This gene has multiple pseudogenes.
3-phosphoinositide-dependent protein kinase 1
, 3-phosphoinositide dependent protein kinase-1
, pkB kinase
, protein kinase B kinase
, PkB kinase like gene 1
, Pkb kinase
, ATP synthase c subunit
, ATP synthase lipid-binding protein, mitochondrial
, ATP synthase proteolipid P2
, ATP synthase, H+ transporting, mitochondrial F0 complex, subunit C2 (subunit 9)
, ATP synthase, H+ transporting, mitochondrial F0 complex, subunit c (subunit 9)
, ATPase protein 9
, ATPase subunit C
, mitochondrial ATP synthase, subunit C (subunit 9)
, phosphoinositide dependent kinase 1
, phosphoinositide-dependent kinase 1
, protein kinase 61C
, serine/threonine protein kinase
, pyruvate dehydrogenase kinase 1
, pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 1, mitochondrial