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mechanism
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40 values
effect
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10 values
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1.63k
signor_id
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14
P29317
O43921
0
binding
up-regulates
0.816
Ephrin-a ligands (named ephrin-a1_ephrin-a5) are anchored in the plasma membrane through a gpi-linkage, and each can bind any of the epha subclass of receptors (epha1_epha8)
SIGNOR-65413
P35638
P18848
0
transcriptional regulation
up-regulates quantity by expression
0.816
ATF4 also induces another bZIP protein C/EBP-homologous protein (CHOP), which is responsible for triggering apoptosis in cells under prolonged ER stress. ATF4 and CHOP further induce growth arrest and DNA damage–inducible protein 34 (GADD34),a regulatory subunit of protein phosphatase 1 (PP1) that dephosphorylates eIF2α. This negative feedback mechanism enables protein synthesis to resume after resolution of ER stress.
SIGNOR-260170
P27037
P08476
0
binding
up-regulates activity
0.815
A protein of 494 amino acids comprising a ligand-binding extracellular domain, a single membrane-spanning domain, and an intracellular kinase domain with predicted serine/threonine specificity. 125I-activin A binds to transfected COS cells with an affinity of 180 pM and can be competed by activin A, activin B, and inhibin A, but not by transforming growth factor beta 1.
SIGNOR-235138
Q9Y6K9
O43318
0
binding
up-regulates activity
0.815
This result suggests that ikkgamma/nemo binds to the polyubiquitinated tak1.
SIGNOR-162634
O43592
P62826
0
binding
up-regulates activity
0.815
The first step in export appears to be the formation of a trimeric tRNA/exportin-t/RanGTP complex. tRNA and RanGTP bind to exportin-t in a highly cooperative manner: tRNA increases the affinity of exportin-t for RanGTP apparently 300-fold (Figure 5A); conversely, RanGTP has to increase the affinity of exportin-t for tRNA by the same factor. RanGTP appears to have at least two functions in this complex. First, it stabilizes the tRNA/exportin-t interaction (see Figure 4B). Second, exportin-t apparently has to bind RanGTP for rapid exit from the nucleus
SIGNOR-261392
O14746
O60832
0
binding
up-regulates activity
0.815
Dyskerin was recently found to be associated with active human telomerase (34), and mutations in dyskerin or NOP10 or deletion of the H/ACA motif of hTERC result in diminished telomerase activity
SIGNOR-263332
Q13535
Q92547
0
binding
up-regulates activity
0.814
These results establish that TopBP1 can activate both Xenopus and human ATR. Furthermore, these experiments provide conclusive evidence that the kinase activity that is induced by TopBP1 is intrinsic to the ATR protein itself and is not due to a kinase that associates with ATR.
SIGNOR-263232
P23528
P53667
0
phosphorylation
down-regulates
0.814
Our results suggest that limk1-mediated cofilin phosphorylation is required for accurate spindle orientation by stabilizing cortical actin networks during mitosis
SIGNOR-159885
P29317
P52797
0
binding
up-regulates
0.814
The eph family of receptors.
SIGNOR-52309
P12644
Q13253
0
binding
down-regulates
0.814
Noggin acts by binding bmps, thus preventing them from binding to their receptors (180). Noggin binds with various degrees of affinity bmp-2, -4, -5, -6, and -7, gdf-5, gdf-6, and vg1, but not other members of the tgf- family of peptides
SIGNOR-100660
Q7Z434
Q9BYX4
0
binding
up-regulates activity
0.814
Initially, RIG-I and MDA5 sense dsRNA in the cytoplasm, produced as a by-product of RNA virus replication.Once one or both of these sensors are activated, they interact with a mitochondrial membrane protein called MAVS (mitochondrial antiviral) (also called IPS1, Cardif, and VISA). They signal to the mitochondrial membrane protein MAVS, which in turn activates the kinases TBK1 and IKKɛ.
SIGNOR-260140
P48357
P41159
0
binding
up-regulates
0.814
Both ob-ra and ob-rb bind leptin with the same affinity, whereas only ob-rb can elicit intracellular response
SIGNOR-55656
Q16236
Q14145
0
ubiquitination
down-regulates quantity
0.813
Keap1 is a substrate receptor of a Cul3-RING ubiquitin ligase (CRL3) that, in physiological conditions, constitutively binds and targets Nrf2 for degradation
SIGNOR-259335
P49736
Q9H211
0
binding
up-regulates activity
0.813
Chromosomal DNA replication requires the recruitment of the six-subunit minichromosome maintenance (Mcm) complex to chromatin through the action of Cdc6 and Cdt1.
SIGNOR-261681
P27986
P35568
0
binding
up-regulates activity
0.813
Phosphorylated irs then acts as docking site to recruit and activate phosphatidylinositol-3-kinase (pi3k) which phosphorylates membrane phospholipids, generating phosphoinositide-3,4,5-triphosphate (pip3) from phosphoinositide-4,5-biphosphate (pip2).
SIGNOR-175668
Q8NHV4
Q7Z4H7
0
binding
up-regulates activity
0.813
FAM29A recruits NEDD1 to spindle MTs. Ectopically expressed NEDD1 and FAM29A interact with each other.
SIGNOR-261421
P32241
P18509
0
binding
up-regulates
0.813
Pacap binds to a pacap-specific receptor (pac1) and to vpac receptors (vpac1 and vpac2), which share high affinity for vasoactive intestinal polypeptide (vip).
SIGNOR-116066
P01112
P21359
0
gtpase-activating protein
down-regulates activity
0.813
Nf1encodes neurofibromin, a protein with multiple functions including ras inactivation (ras gtpase-activating protein or rasgap) and adenylyl cyclase (ac) activation
SIGNOR-204357
Q13315
Q92878
0
binding
up-regulates
0.813
One of the earliest events is recruitment and activation of the atm at the damaged dna sites through the mre11rad50nbs1 (mrn) sensor complex. . the mre11/rad50/nbs1 (mrn) complex maintains genomic stability by bridging dna ends and initiating dna damage signaling through activation of the atm kinase.
SIGNOR-175053
P19235
O60674
0
phosphorylation
up-regulates activity
0.812
JAK2 in turn phosphorylates several tyrosine residues on the EpoR-cytosolic domain and probably on JAK2 itself that serve as docking sites for SH2 or protein tyrosine binding domains of downstream signal transduction proteins such as STAT5, phosphatidylinositol 3-kinase, Shc, and tyrosine phosphatases SHP1 and SHP2
SIGNOR-251351
Q99661
P53350
0
phosphorylation
up-regulates activity
0.812
Active PLK1, in turn, phosphorylates MCAK at Ser715 which promotes its microtubule depolymerase activity essential for faithful chromosome segregation.
SIGNOR-276931
P51587
Q9BXW9
0
binding
up-regulates activity
0.812
Fanconi anemia complementation group FANCD2 protein serine 331 phosphorylation is important for fanconi anemia pathway function and BRCA2 interaction
SIGNOR-263238
P22681
P06241
0
phosphorylation
up-regulates activity
0.812
Fyn associates with cbl and phosphorylates tyrosine 731 in cbl, a binding site for phosphatidylinositol 3-kinasecbl represents a substrate for src-like kinases that are activated in response to the engagement of cell surface receptors, and that src-like kinases are responsible for the phosphorylation of a tyrosine residue in cbl that may regulate activation of phosphatidylinositol 3-kinase
SIGNOR-63968
P50570
Q9Y5X1
0
binding
up-regulates
0.812
Snx9 binds directly to bothdynamin-1 anddynamin-2. Moreover by stimulatingdynaminassembly, snx9 stimulatesdynamin's basal gtpase activity and potentiates assembly-stimulated gtpase activity on liposomes.
SIGNOR-133976
P84022
P36897
0
phosphorylation
up-regulates activity
0.812
A major event leading to Smad3 activation is the TGF-beta-induced, TbetaRI-mediated phosphorylation at two C-terminal serine residues, Ser-423 and Ser-425, which triggers dissociation of Smad3 from its receptors to form a complex with Smad4 and accumulate in the nucleus
SIGNOR-235380
Q15375
P20827
0
binding
up-regulates
0.812
The best known function is their role in the guidance of migration of axons and cells in the nervous system through repulsive interactions
SIGNOR-56965
P60953
P46940
0
binding
down-regulates activity
0.811
Although the name implies that it functions as a GTPase-activating protein, IQGAP1 actually stabilizes Cdc42 and Rac1 in the active, GTP-bound form (5, 8, 17). Thus, IQGAP1 acts as an “anti-GTPase-activating protein” for Cdc42 and Rac1, with marked effects on the cytoskeleton. 
SIGNOR-261888
P54756
P52798
0
binding
up-regulates
0.811
Receptors of the epha group preferentially interact with glycosylphosphatidylinositol (gpi)-linked ligands (of the ephrin-a subclass, which comprises five ligands), while receptors of the ephb group preferentially interact with transmembrane ligands (of the ephrin-b subclass, which comprises three ligands) (table 1). In either case, binding of a ligand results in eph receptor autophosphorylation on tyrosine residues and activation of the kinase activity of the eph receptor
SIGNOR-52430
P63000
P52565
0
guanine nucleotide exchange factor
down-regulates activity
0.811
Here, we report the expression of plexin-B3 in glioma cells, which upon stimulation by its ligand Sema5A results in significant inhibition of cell migration and invasion. A search for the underlying mechanism revealed direct interaction of plexin-B3 with RhoGDP dissociation inhibitor α (RhoGDIα), a negative regulator of RhoGTPases that blocks guanine nucleotide exchange and sequesters them away from the plasma membrane. direct interaction of RhoGDIα and the cytoplasmic domain of plexin-B3 (plexin-B3CD) was confirmed by GST pulldown assays.RhoGDIα is required for Sema5A-induced Rac1 inactivation and inhibition of cell invasion in C6 glioma.
SIGNOR-268436
P61224
Q8WZA2
0
guanine nucleotide exchange factor
up-regulates activity
0.811
Epac1 (cAMP-GEFI) and Epac2 (cAMP-GEFII) are closely related guanine nucleotide exchange factors (GEFs) for the small GTPase Rap1, which are directly regulated by cAMP. Here we show that both GEFs efficiently activate Rap2 as well.
SIGNOR-263955
Q00987
P31749
0
phosphorylation
up-regulates quantity by stabilization
0.811
Mitogen-induced activation of phosphatidylinositol 3-kinase (pi3-kinase) and its downstream target, the akt/pkb serine-threonine kinase, results in phosphorylation of mdm2 on serine 166 and serine 186. Phosphorylation on these sites is necessary for translocation of mdm2 from the cytoplasm into the nucleus.Both akt expression and serum treatment induced phosphorylation of mdm2 at ser186.
SIGNOR-116270
P42229
Q15303
0
phosphorylation
up-regulates activity
0.811
ERBB4 directly activates STAT5A, in part, through phosphorylation of STAT5A at the regulatory Tyr-694.|ERBB4/HER4 potentiates STAT5A transcriptional activity by regulating novel STAT5A serine phosphorylation events.
SIGNOR-279711
Q9UF33
P20827
0
binding
up-regulates
0.811
Ephrin-a1 binds and activates the tyrosine kinase activity of eph-a2, and has a dissociation constant of 20_30 nm. ephrin-a1 interacts with all the other epha subclass receptors as well, although with different affinity
SIGNOR-56962
Q12879
P78352
0
relocalization
up-regulates activity
0.811
The PDZ domains of PSD-95 and related proteins interact with the COOH-terminal sequences of K+channels and NMDA2 receptors (3). By these interactions, PSD-95 may mediate the clustering of K+ channels and NMDA receptors at synapses.
SIGNOR-264194
P54756
P20827
0
binding
up-regulates
0.811
Ephrin-a1 binds and activates the tyrosine kinase activity of eph-a2, and has a dissociation constant of 20_30 nm. ephrin-a1 interacts with all the other epha subclass receptors as well, although with different affinity
SIGNOR-56910
O95140
Q9BXM7
0
phosphorylation
down-regulates quantity
0.81
If PINK1 is responsible for the degradation of Mfn2, then silencing PINK1 should induce mitochondrial fusion by upregulating Mfn2 expression.|We show that downregulation of Mfn2 is induced by proteasomal degradation triggered by PINK1, which phosphorylates Mfn2 at S442.
SIGNOR-278208
P27986
P00533
0
binding
up-regulates
0.81
The egf-r coimmunoprecipitated with p85 alpha
SIGNOR-121959
Q12778
Q96EB6
0
deacetylation
down-regulates quantity by destabilization
0.81
SIRT1 overexpression reduces muscle wasting by blocking the activation of FoxO1 and 3
SIGNOR-217975
Q13464
P61586
0
binding
up-regulates activity
0.81
Planar cell polarity (pcp) signalling triggers activation of the small gtpases rhoa and rac1, which in turn activate rho kinase (rock) and jun-n-terminal kinase (jnk), respectively, leading to actin polymerization and microtubule stabilization.
SIGNOR-199542
P12643
Q13253
0
binding
down-regulates
0.81
Noggin acts by binding bmps, thus preventing them from binding to their receptors (180). Noggin binds with various degrees of affinity bmp-2, -4, -5, -6, and -7, gdf-5, gdf-6, and vg1, but not other members of the tgf- family of peptides
SIGNOR-100657
P61073
P48061
0
binding
up-regulates
0.809
To study the role of the sdf-1/cxcr4-chemokine/receptor system as a regulator of vertebrate development, we isolated and characterized a cdna encoding sdf-1 of the lower vertebrate xenopus laevis (xsdf-1). Recombinant xsdf-1 was produced in insect cells, purified, and functionally characterized. Although xsdf-1 is only 64-66% identical with its mammalian counterparts, it is indistinguishable from human (h)sdf-1alpha in terms of activating both x. laevis cxcr4 and hcxcr4. Thus, both xsdf-1 and hsdf-1alpha promoted cxcr4-mediated activation of heterotrimeric g(i2) in a cell-free system and induced release of intracellular calcium ions in and chemotaxis of intact lymphoblastic cells.
SIGNOR-115029
P04792
P49137
0
phosphorylation
down-regulates
0.809
Notably mk2 is well known to play an important role in actin filament remodellng by phosphorylating hsp27.
SIGNOR-94021
Q9Y219
Q96AX9
0
ubiquitination
up-regulates
0.809
Skeletrophin bound the intracellular regions of the notch ligand jagged-2, but not to those of delta-1, -3, -4, or jagged-1. Skeletrophin, but not its ring-mutated form, ubiquitinized the intracellular region of jagged-2.
SIGNOR-137922
Q8IZF0
Q8N2C7
0
binding
up-regulates activity
0.809
The NALCN complex in the brain consists of NALCN, UNC80 and UNC79. UNC80 directly associates with NALCN and UNC79 forms part of the complex by its interaction with UNC80.
SIGNOR-265184
P15927
Q13315
0
phosphorylation
up-regulates
0.809
Replication protein a (rpa) is a single-stranded dna (ssdna) binding protein involved in various processes, including nucleotide excision repair and dna replication. The 32 kda subunit of rpa (rpa32) is phosphorylated in response to various dna-damaging agents, and two protein kinases, ataxia-telangiectasia mutated (atm) and the dna-dependent protein kinase (dna-pk) have been implicated in dna damage-induced phosphorylation of rpa32we show that both dna-pk and atm phosphorylate rpa32 on thr21 in vitro.
SIGNOR-121861
Q8NEB9
Q9P2Y5
0
binding
up-regulates activity
0.809
Although both human atg14 and uvrag interact with beclin 1 and vps34.
SIGNOR-181554
P49023
P12931
0
phosphorylation
up-regulates activity
0.808
Here, we demonstrate that Src kinase directly phosphorylates Y88 paxillin|In this study, we also show how pY88 paxillin transduces a signal to activate Akt
SIGNOR-263977
P49917
P78527
0
phosphorylation
down-regulates
0.808
Using tandem mass spectrometry, we identified a dna-pk phosphorylation site at thr-650 in human lig4 and a potential second phosphorylation site at ser-668 or ser-672. Phosphorylation of lig4 per se was not required for lig4 dna end joining activity. Substitution of these amino acids with alanine, individually or in combination, led to changes in lig4 protein stability of mouse lig4. The phosphomimetic mutation s650d returned lig4 stability to that of the wild-type protein. Furthermore dna-pk was found to negatively regulate lig4 protein stability.
SIGNOR-125877
P35222
P49768
0
binding
down-regulates
0.808
Importantly, our data show that binding of ps1 to cadherin mediates the effects of ps1 on the phosphorylation, ubiquitination, and destabilization of beta-catenin. Thus, cadherins mediate both the association of ps1 and beta-catenin and the effects of ps1 on the cellular levels of beta-catenin
SIGNOR-22837
Q04721
Q92585
0
binding
up-regulates
0.808
Maml1 binds to the ankyrin repeat domain of all four mammalian notch receptors, forms a dna-binding complex with icn and rbp-jkappa, and amplifies notch-induced transcription of hes1.
SIGNOR-84835
Q07817
Q13323
0
binding
down-regulates
0.808
We have identified a novel cellular protein, bik, that interacts with the cellular survival-promoting proteins, bcl-2 and bcl-xl in transient transfection assays, bik promotes cell death in a manner similar to the death-promoting members of the bcl-2 family, bax and bak.
SIGNOR-26453
Q9BY84
P28482
0
phosphorylation
up-regulates quantity by stabilization
0.808
Phosphorylation of Ser-446 determines stability of MKP-7.|We also determined that MKP-7 phosphorylated at Ser-446 has a longer half-life than unphosphorylated form of the wild type protein, as does a phospho-mimic mutant of MKP-7. These results indicate that activation of the ERK pathway strongly blocks JNK activation through stabilization of MKP-7 mediated by phosphorylation.
SIGNOR-249389
Q15562
Q9GZV5
0
binding
up-regulates
0.808
When dephosphorylated, yap/taz enter nuclei and induce gene transcription by interacting with transcription factors tead14.
SIGNOR-201382
O43157
Q92854
0
binding
up-regulates
0.808
Binding of sema 4d to plexin b1 stimulates the tyrosine kinase activity of met, resulting in tyrosine phosphorylation of both receptors.
SIGNOR-92201
Q9HC77
Q66GS9
0
binding
up-regulates activity
0.808
In this study, we demonstrate that the human microcephaly protein, CEP135, directly interacts with hSAS-6 via its carboxyl-terminus and with MTs via its amino-terminus. Unexpectedly, CEP135 also interacts with another microcephaly protein CPAP via its amino terminal domain. Depletion of CEP135 not only perturbed the centriolar localization of CPAP, but also blocked CPAP-induced centriole elongation. We propose that CEP135 may serve as a linker protein that directly connects the central hub protein, hSAS-6, to the outer MTs, and suggest that this interaction stabilizes the proper cartwheel structure for further CPAP-mediated centriole elongation.
SIGNOR-269677
P19174
O43561
0
binding
up-regulates activity
0.808
By substituting these tyrosine residues in LAT with phenylalanine and by utilizing phosphorylated peptides derived from these sites, we mapped the tyrosine residues in LAT required for the direct interaction and activation of Vav, p85/p110alpha and phospholipase Cgamma1 (PLCgamma1). Our results indicate that Tyr(226) and Tyr(191) are required for Vav binding, whereas Tyr(171) and Tyr(132) are necessary for association and activation of phosphoinositide 3-kinase activity and PLCgamma1 respectively.
SIGNOR-246060
P14653
P40424
0
binding
up-regulates activity
0.807
Pbx1 and exd act as cofactors that enhance the DNA binding specificity of Hox proteins. The structure of the HoxB1–Pbx1–DNA ternary complex shows that HoxB1 and Pbx1 bind to overlapping binding sites located on opposite faces of the DNA.
SIGNOR-241219
O15534
P48730
0
phosphorylation
down-regulates quantity by destabilization
0.807
Human casein kinase Idelta phosphorylation of human circadian clock proteins period 1 and 2. We have now extended our previous studies to show that human casein kinase Idelta (hCKIdelta), the closest homologue to hCKIepsilon, associates with and phosphorylates hPER1 and causes protein instability. Furthermore, we observed that both hCKIdelta and hCKIepsilon phosphorylated and caused protein instability of human period 2 protein (hPER2).
SIGNOR-268001
P28749
P11802
0
phosphorylation
up-regulates activity
0.807
Here we assessed the effects of alanine substitution at the individual or combined Cdk4(6)-specific sites in p130, compared with homologous sites in p107 (Thr(369)/Ser(650)/Ser(964)). In U-2-OS cells, the triple p107(DeltaCdk4)* mutant strongly inhibited E2F-4 activity and imposed a G(1) arrest resistant to cyclin D1 coexpression. 
SIGNOR-250764
Q92569
P08069
0
binding
up-regulates
0.807
Moreover, we found that the insulin-like growth factor-1 receptor (igf-ir) bound to p55pik;the interaction occurred at the receptor tyrosine 1316 and involved both p55pik sh2 domains.
SIGNOR-52683
P14780
P01033
0
binding
down-regulates activity
0.807
Tissue inhibitor of metalloproteinase (TIMP-1) is an inhibitor of MMP-9 that binds to MMP-9 precursors and to the active form.
SIGNOR-278116
Q04771
P18075
0
binding
up-regulates
0.807
Bmp-4 and gdf-5 are known to bind to activin receptor-like kinase 3 (alk-3) and/or alk-6 (also termed bmp type ia and type ib receptors, respectively), whereas bmp-6 and bmp-7 preferentially bind to alk-2
SIGNOR-236913
P29353
P04626
0
binding
up-regulates
0.807
Shc interacts with and is an excellent substrate for erbb2 and appears to play an important role in mitogenic signaling through this receptor tyrosine kinase
SIGNOR-65579
P42262
Q9NRD5
0
binding
up-regulates activity
0.807
RAB39B directs GluA2 trafficking in neurons. GTP-bound RAB39B interacts with PICK1. In line with evidence that PICK1 can dimerize, the structural model suggests that dimerization of PICK1 is a prerequisite for simultaneous recognition of both RAB39B and GluA2 each by one of the PICK1 molecules in the PICK1 dimer (Fig. 6a–c). The existence of such complex is supported by our co-immunoprecipitation experiments shown above.
SIGNOR-264046
P10242
Q92793
0
binding
up-regulates activity
0.807
the nuclear co-activator CREB binding protein (CBP). This protein interacts directly with both c-Myb and v-Myb and potentiates Myb-specific transcription
SIGNOR-240994
Q8WV28
P43405
0
phosphorylation
up-regulates
0.806
The phosphorylation of multiple tyrosine residues not only amplifies plcgamma-mediated signaling but also supports 'cis'-mediated interaction between distinct signaling effectors within a large molecular complex.
SIGNOR-96044
P61586
Q92974
0
guanine nucleotide exchange factor
up-regulates activity
0.806
We therefore developed a screening-compatible live-cell imaging assay, using FRET-based biosensors for the prototype GTPases RHOA, RAC1 and CDC4215,19,20 (Extended Data Fig. 2 and Supplementary Note 1)|We found catalytic activities for 45/75 RhoGEFs and 48/63 RhoGAPs| Our data thus not only reveal extensive promiscuity among regulators, but also that the inactivating RhoGAPs are less selective than the activating RhoGEFs (p-value=0.02)(Supplementary Table 2).
SIGNOR-260529
Q15375
O43921
0
binding
up-regulates
0.806
The activation of eph receptors by their ligands, which are membrane-anchored molecules, involves a cell-cell recognition event that often causes cell repulsion.
SIGNOR-52206
P15172
P15923
0
binding
up-regulates activity
0.806
In addition we demonstrate that myod, in conjunction with e12/e47-like proteins, is functioning as a regulatory nodal point for activation of several other downstream muscle regulators.
SIGNOR-20540
Q969F8
Q15726
0
binding
up-regulates
0.806
Here we show that kiss-1 (refs 1, 4) encodes a carboxy-terminally amidated peptide with 54 amino-acid residues, which we have isolated from human placenta as the endogenous ligand of an orphan g-protein-coupled receptor (hot7t175) and have named 'metastin'
SIGNOR-108480
P35222
O14640
0
binding
up-regulates activity
0.806
Activated DVL binds and inhibits the phosphorylation of beta-catenin by GSK3B, blocking beta-catenin degradation so that beta catenin accumulates and translocates to the nucleus, where it interacts with the t cell specific factor (tcf)/lymphoid enhancer binding factor 1 (lef-1) transcription factor and induces the transcription of target genes such as c-jun, c-myc, and cyclin d1.
SIGNOR-134285
P42224
O60674
0
phosphorylation
up-regulates
0.806
Phosphorylation at tyr701 by the janus family of tyrosine kinases (jak) leads to stat1 dimerization via its src homology 2 domains, exposure of a dimer-specific nuclear localization signal, and subsequent nuclear translocation.
SIGNOR-235709
Q13043
Q9NS23
0
binding
up-regulates
0.806
Rassf1a and mst1 co-exist as a complex localizing at microtubules throughout the cell cycle, of which the rassf1a mst1 interaction is stimulatory to the mst1 kinase activity.
SIGNOR-197744
Q16671
P03971
0
binding
up-regulates
0.806
The results point to anti-m?llerian Hormone (amh) being the most likely candidate ligand for c14.
SIGNOR-36215
Q9UDY8
Q9BXL7
0
binding
up-regulates
0.805
The carboxy-terminal part of the bcl10 card and a short stretch of 13 amino acids following the card are required for constitutive binding to malt1.
SIGNOR-167393
Q15628
P19438
0
binding
up-regulates activity
0.805
We have identified a novel 34 kda protein, designated tradd, that specifically interacts with an intracellular domain of tnfr1 tradd interacts with the death domain of tnfrsf1a to initiate distinct signaling cascades for two of the most important biological activities of tnf, nf-kb activation and programmed cell death tradd, a novel protein that specifically interacts with the death domain of tnfr1 and activates signaling pathways for both of these activities when overexpressed.
SIGNOR-32739
P01130
P04114
0
binding
up-regulates
0.805
In the case of ldl, binding of apolipoprotein b (apob) to the ldl-r18-20 and proteoglycans17 21 initiates plasma clearance and lipoprotein degradation
SIGNOR-87035
P84022
Q96PU5
0
ubiquitination
down-regulates activity
0.805
Through its ww domain, nedd4l specifically recognizes a tgf-beta-induced phosphothr-protyr motif in the linker region, resulting in smad2/3 polyubiquitination and degradation
SIGNOR-232104
P35222
P31749
0
phosphorylation
up-regulates
0.805
Phosphorylation of beta-catenin by akt promotes beta-catenin transcriptional activity|we have demonstrated that akt phosphorylates beta-catenin at ser552 in vitro and in vivo.
SIGNOR-252499
P20336
Q86UR5
0
relocalization
up-regulates activity
0.805
N-terminal interactions of RIMs with RAB3 and MUNC13 regulate DCV fusion. Through N-terminal interactions, RIMs position MUNC13 and recruit DCVs via RAB3, which is located on the vesicle
SIGNOR-264381
P51686
O15444
0
binding
up-regulates
0.805
Ccr9 is a specific receptor for the beta-chemokine teck/ccl25.
SIGNOR-104902
Q16539
Q9BY84
0
dephosphorylation
down-regulates
0.805
Mkp-7 binds to and inactivates p38 mapk and jnk/sapk, but not erk inhibited by dual specificity phosphatases, such as dusp1, dusp10, and dusp16(uniprot)
SIGNOR-108233
P06730
P11940
0
binding
up-regulates activity
0.805
The binding of PABP to mRNA poly(A) tails is followed by interactions with eukaryotic initiation factor (eIF4G) and other translation factors, including eIF4E, to constitute a translation initiation complex, which mediates cellular mRNA circularization and enhances cap-dependent translation by facilitating ribosome recycling
SIGNOR-260968
P00751
P00746
0
cleavage
up-regulates activity
0.804
The resulting proconvertase C3bB is subsequently cleaved by factor D (FD), generating the AP C3 convertase C3bBb
SIGNOR-263488
Q13873
P18075
0
binding
up-regulates
0.804
In transfected cos-1 cells, osteogenic protein (op)-1/bmp-7, and less efficiently bmp-4, bound to bmpr-ii. Bmpr-ii bound ligands only weakly alone, but the binding was facilitated by the presence of previously identified type i receptors for bmps. Binding of op-1/bmp-7 to bmpr-ii was also observed in nontransfected cell lines. Moreover, a transcriptional activation signal was transduced by bmpr-ii in the presence of type i receptors after stimulation by op-1/bmp-7.
SIGNOR-30512
P62993
O43561
0
binding
up-regulates
0.804
Phosphorylated tyrosines 171, 191, and 226 [in LAT] bind to the SH2 domains of the Grb2 family of adaptor proteins and must be present for optimal signalling
SIGNOR-251520
Q13094
P43403
0
phosphorylation
up-regulates
0.804
Zap-70 phosphorylates slp-76 at specific sites that allow vav sh2 domain bindingwe also show by in vitro and in vivo analysis that two slp-76 pyesp motifs (y113 and y128) mediate binding, the first being more efficient.
SIGNOR-46859
P30307
P53350
0
phosphorylation
up-regulates
0.804
The nuclear accumulation of active m-phase promoting factor (mpf) during prophase is thought to be essential for coordinating m-phase events in vertebrate cells. The protein phosphatase cdc25c, an activator of mpf, enters the nucleus to keep mpf active in the nucleus during prophase. these results suggest that plk1 phosphorylates cdc25c on ser198 and regulates nuclear translocation of cdc25c during prophase.
SIGNOR-115993
P29320
P52797
0
binding
up-regulates
0.804
The activation of eph receptors by their ligands, which are membrane-anchored molecules, involves a cell-cell recognition event that often causes cell repulsion. transmembrane ligands for eph receptors also exhibit properties of signal transducing molecules, suggesting that bidirectional signaling occurs when receptor-expressing cells contact ligand-expressing cells.
SIGNOR-52312
P56945
P12931
0
phosphorylation
up-regulates activity
0.803
Cas is a member of the focal adhesion complex. Phosphorylation of Cas by Src is an important event leading to cell transformation. Using mass spectrometry, we have mapped 11 sites in Cas that are phosphorylated by Src. These sites are all located between residues 132 and 414 of CasBased on these data, 11 tyrosine residues (132, 169, 183, 196, 238, 253, 271, 291, 301, 391, and 414) were phosphorylated by Src|the biological activity of Cas depends on its phosphorylation by Src (16–18). After phosphorylation, Cas associates with a number of proteins, including Crk, Src, phosphatidylinositol 3-kinase, Nck, and phospholipase Cgamma, via SH2 binding motifs
SIGNOR-246393
O95786
Q14258
0
ubiquitination
up-regulates activity
0.803
Lys63 linked polyubiquitination of RIG-I at Lys 172 catalyzed by TRIM25 is an important step for RIG-I activation.
SIGNOR-278730
Q9GZQ8
Q9Y4P1
0
cleavage
up-regulates
0.803
Human atg4 homologues cleave the carboxyl termini of the three human atg8 homologues, microtubule-associated protein light chain 3 (lc3), gabarap, and gate-16.
SIGNOR-125449
P54274
O95271
0
ADP-ribosylation
down-regulates activity
0.803
Tankyrase 1 ADP-ribosylates TRF1, inhibiting its binding to telomeric DNA.
SIGNOR-263377
P62993
P35568
0
binding
up-regulates activity
0.803
Association ofinsulinreceptor substrate 1 (irs-1) y895 with grb-2 mediates theinsulinsignaling involved in irs-1-deficient brown adipocyte mitogenesis.
SIGNOR-236614
P78352
Q9Y2H0
0
binding
up-regulates activity
0.803
SAPAPs are specifically expressed in neuronal cells and enriched in the PSD fraction. SAPAPs induce the enrichment of PSD-95/SAP90 to the plasma membrane in transfected cells. Thus, SAPAPs may have a potential activity to maintain the structure of PSD by concentrating its components to the membrane area.
SIGNOR-264212
Q9ULT6
Q2MKA7
0
relocalization
down-regulates quantity
0.803
Mechanistically, R-spondin interacts with the extracellular domain of ZNRF3 and induces the association between ZNRF3 and LGR4, which results in membrane clearance of ZNRF3. These data suggest that R-spondin enhances Wnt signalling by inhibiting ZNRF3.
SIGNOR-260113
P04637
Q96EB6
0
deacetylation
down-regulates
0.803
Sirt1 has been shown to regulate cell fate in part by deacetylating the p53 protein at lysine 382 and inhibiting p53-mediated transcriptional activation and apoptosis.
SIGNOR-182515
Q9P2D8
Q8N2C7
0
binding
up-regulates activity
0.803
The NALCN complex in the brain consists of NALCN, UNC80 and UNC79. UNC80 directly associates with NALCN and UNC79 forms part of the complex by its interaction with UNC80.
SIGNOR-265183
Q9Y6C5
Q15465
0
binding
down-regulates activity
0.803
Biochemical analysis of ptch and ptch2 shows that they both bind to all hedgehog family members with similar affinity and that they can form a complex with smo.Current models suggest that binding of Shh to PTCH prevents the normal inhibition of the seven-transmembrane-protein Smoothened (SMO) by PTCH.
SIGNOR-217776
Q15109
P09429
0
binding
up-regulates activity
0.803
HMGB1 is known to influence cellular responses within the nervous system via two distinct receptor families; the Receptor for Advanced Glycation End-products (RAGE) and Toll-like receptors (TLRs)
SIGNOR-252059