Parameter | Value |
---|---|
Gene | Gabbr1 |
Protein Name | GABR1_RAT |
Organism | Rattus norvegicus (Rat) |
Alternative name(s) | Gamma-aminobutyric acid type B receptor subunit 1 (GABA-B receptor 1) (GABA-B-R1) (GABA-BR1) (GABABR1) (Gb1) |
Protein Family | G-protein coupled receptor 3 family |
NCBI Gene ID | 81657 |
UniProt ID | Q9Z0U4 |
Enzyme Class | - |
Molecular Weight | 111534 |
Protein Length | 991 |
Protein Domain | InterPro | Pfam |
3D Structure |
PDBe |
PDBj |
RCSB PDB |
DrugPort
ModBase | SwissModel |
Gene Expression | Gene Expression Atlas |
Function and Disease | OMIM |
Protein-protein Interaction Database | STRING | IntAct | MINT |
Kinase Database | Phospho.ELM | PhosphoSite | NetworKIN |
Catalytic Activity (UniProt annotation) | - |
Localization | Cell membrane |
Function (UniProt annotation) | Component of a heterodimeric G-protein coupled receptor for GABA, formed by GABBR1 and GABBR2 (PubMed:9872315, PubMed:9872317, PubMed:9872744). Within the heterodimeric GABA receptor, only GABBR1 seems to bind agonists, while GABBR2 mediates coupling to G proteins (PubMed:9872317, PubMed:10658574). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase (PubMed:10075644, PubMed:9872315, PubMed:9872744, PubMed:10924501). Signaling inhibits adenylate cyclase, stimulates phospholipase A2, activates potassium channels, inactivates voltage-dependent calcium-channels and modulates inositol phospholipid hydrolysis (PubMed:9069281, PubMed:10457184, PubMed:9872315, PubMed:9872744, PubMed:10924501, PubMed:10692480). Calcium is required for high affinity binding to GABA (PubMed:10692480). Plays a critical role in the fine-tuning of inhibitory synaptic transmission (PubMed:9872744). Pre-synaptic GABA receptor inhibits neurotransmitter release by down-regulating high-voltage activated calcium channels, whereas postsynaptic GABA receptor decreases neuronal excitability by activating a prominent inwardly rectifying potassium (Kir) conductance that underlies the late inhibitory postsynaptic potentials (PubMed:9872744, PubMed:10924501, PubMed:10692480). Not only implicated in synaptic inhibition but also in hippocampal long-term potentiation, slow wave sleep, muscle relaxation and antinociception (By similarity). |
Gene Ontology | GO:0001649; GO:0004965; GO:0005615; GO:0005789; GO:0005887; GO:0007193; GO:0007194; GO:0007214; GO:0008021; GO:0008134; GO:0008285; GO:0014048; GO:0014049; GO:0014053; GO:0030054; GO:0030673; GO:0031966; GO:0032811; GO:0033602; GO:0035094; GO:0038039; GO:0043005; GO:0043025; GO:0043197; GO:0043198; GO:0043204; GO:0043231; GO:0045121; GO:0045471; GO:0046982; GO:0050805; GO:0060124; GO:0097060; GO:0098978; GO:0098982; GO:0099055; GO:0099056; GO:1902710; GO:1990430 |
Gene Name | Organism | P-Site | Sequence(+/-7) | Conservation | Disorder | Curator Assessment | Reliability | Evidence Class | Evidence Logic | PubMed | Phospho-ELM | PhosphoSite-Plus |
---|---|---|---|---|---|---|---|---|---|---|---|---|
PRKAA1 (Q13131) | Homo sapiens | S948 | ELRHQLQSRQQLRSR | N/A | 0.6427 | - | - | - | - | - | - |
|
Reactome Pathways
KEGG Pathways
Pathway ID | Pathway Name |
---|---|
rno04080 | Neuroactive ligand-receptor interaction |
No NCI Nature pathways found