| + |
PRKCD | up-regulates activity 
phosphorylation
|
GRM5 |
0.353 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249280 |
Ser840 |
VRSAFTTsTVVRMHV |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249287 |
Thr841 |
RSAFTTStVVRMHVG |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Publications: |
2 |
Organism: |
In Vitro |
| + |
PRKCZ | up-regulates activity
phosphorylation
|
GRM5 |
0.377 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249284 |
Ser840 |
VRSAFTTsTVVRMHV |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249291 |
Thr841 |
RSAFTTStVVRMHVG |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Publications: |
2 |
Organism: |
In Vitro |
| + |
PRKCQ | up-regulates activity
phosphorylation
|
GRM5 |
0.294 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249283 |
Ser840 |
VRSAFTTsTVVRMHV |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249290 |
Thr841 |
RSAFTTStVVRMHVG |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Publications: |
2 |
Organism: |
In Vitro |
| + |
PRKCA | up-regulates activity
phosphorylation
|
GRM5 |
0.425 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249278 |
Ser840 |
VRSAFTTsTVVRMHV |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249285 |
Thr841 |
RSAFTTStVVRMHVG |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Publications: |
2 |
Organism: |
In Vitro |
| + |
PRKCE | up-regulates activity
phosphorylation
|
GRM5 |
0.405 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249281 |
Ser840 |
VRSAFTTsTVVRMHV |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249288 |
Thr841 |
RSAFTTStVVRMHVG |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Publications: |
2 |
Organism: |
In Vitro |
| + |
PRKCB | up-regulates activity
phosphorylation
|
GRM5 |
0.36 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249279 |
Ser840 |
VRSAFTTsTVVRMHV |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249286 |
Thr841 |
RSAFTTStVVRMHVG |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Publications: |
2 |
Organism: |
In Vitro |
| + |
PRKCG | up-regulates activity
phosphorylation
|
GRM5 |
0.425 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249282 |
Ser840 |
VRSAFTTsTVVRMHV |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-249289 |
Thr841 |
RSAFTTStVVRMHVG |
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Publications: |
2 |
Organism: |
In Vitro |
| + |
glutamic acid | up-regulates activity
chemical activation
|
GRM5 |
0.8 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-264070 |
|
|
Homo sapiens |
|
| pmid |
sentence |
| 25042998 |
Metabotropic glutamate receptors are class C G-protein-coupled receptors which respond to the neurotransmitter glutamate |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
GRM5 | up-regulates activity
binding
|
GNAS |
0.341 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-264078 |
|
|
Homo sapiens |
|
| pmid |
sentence |
| 20055706 |
MGluRs are members of the G-protein-coupled receptor (GPCR) superfamily, the most abundant receptor gene family in the human genome. GPCRs are membrane-bound proteins that are activated by extracellular ligands such as light, peptides, and neurotransmitters, and transduce intracellular signals via interactions with G proteins. The resulting change in conformation of the GPCR induced by ligand binding activates the G protein, which is composed of a heterotrimeric complex of α, β, and γ subunits. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| Tissue: |
Central Nervous System |
| + |
GRM5 | up-regulates 
|
Excitatory_synaptic_transmission |
0.7 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-264348 |
|
|
Homo sapiens |
Neuron |
| pmid |
sentence |
| 24564659 |
Excitatory synaptic transmission in the mammalian brain is mediated primarily by the amino acid glutamate, activating two different groups of glutamate receptors: ionotropic and metabotropic. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
PKC | up-regulates activity
phosphorylation
|
GRM5 |
0.2 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-269972 |
|
|
in vitro |
|
| pmid |
sentence |
| 15894802 |
Thus, we showed that it is phosphorylation of Ser-839, not Thr-840, that is absolutely required for the unique Ca2+ oscillations produced by mGluR5 activation. The Thr-840 residue is important only in that it is permissive for the PKC-dependent phosphorylation of Ser-839. |
|
| Publications: |
1 |
Organism: |
In Vitro |
| + |
GRM5 | up-regulates quantity
relocalization
|
calcium(2+) |
0.8 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-264936 |
|
|
Homo sapiens |
|
| pmid |
sentence |
| 29953871 |
Ca2+ is arguably the most important second messenger in the brain because of its pivotal roles in presynaptic neurotransmitter release, postsynaptic responses, and plasticity induction. iGluRs and mGluRs can generate intracellular Ca2+ signals, albeit by different mechanisms, whose crosstalk has not been thoroughly explored (Figure 2C). iGluRs allow the influx of extracellular Ca2+ upon pore opening. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
ADX-47273 | up-regulates
chemical activation
|
GRM5 |
0.8 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-189338 |
|
|
Homo sapiens |
|
| pmid |
sentence |
| Other |
|
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
3.0
GRM5
- 
- 