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Protein Page:
GABRR1 (human)

Overview
GABRR1 GABA, the major inhibitory neurotransmitter in the vertebrate brain, mediates neuronal inhibition by binding to the GABA/benzodiazepine receptor and opening an integral chloride channel. Rho-1 GABA receptor could play a role in retinal neurotransmission. Belongs to the ligand-gated ion channel (TC 1.A.9) family. Gamma-aminobutyric acid receptor (TC 1.A.9.5) subfamily. GABRR1 sub-subfamily. 2 isoforms of the human protein are produced by alternative splicing. Note: This description may include information from UniProtKB.
Protein type: Channel, chloride; Membrane protein, integral; Channel, ligand-gated; Receptor, misc.
Cellular Component: postsynaptic membrane; integral to plasma membrane; plasma membrane; cell junction
Molecular Function: protein domain specific binding; chloride channel activity; GABA-A receptor activity; protein homodimerization activity; protein heterodimerization activity; extracellular ligand-gated ion channel activity
Biological Process: synaptic transmission; transport; transmembrane transport; gamma-aminobutyric acid signaling pathway
Reference #:  P24046 (UniProtKB)
Alt. Names/Synonyms: bA135P14.1 (gamma-aminobutyric acid (GABA) receptor, rho 1); GABA(A) receptor subunit rho-1; GABRR1; gamma-aminobutyric acid (GABA) A receptor, rho-1; gamma-aminobutyric acid (GABA) receptor, rho 1; Gamma-aminobutyric acid receptor subunit rho-1; GBRR1; MGC163216
Gene Symbols: GABRR1
Molecular weight: 55,883 Da
Basal Isoelectric point: 8.71  Predict pI for various phosphorylation states
Select Structure to View Below

GABRR1

Protein Structure Not Found.


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Modification Sites and Domains  

Modification Sites in Parent Protein, Orthologs, and Isoforms  
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 S166-p FFVHSKRsFIHDttT
0 1 T171-p KRsFIHDttTDNVML
0 1 T172-p RsFIHDttTDNVMLR
0 1 Y219-p CSLEIESyAyTEDDL
0 1 Y221-p LEIESyAyTEDDLML
0 1 Y229-p TEDDLMLyWKKGNDS
1 0 T326 TTVLTMSTIITGVNA
1 0 S334 IITGVNASMPRVSYI
0 1 Y401 TAMLDGNYSDGEVND
0 1 Y412 EVNDLDNYMPENGEK
  mouse

 
S167 FFVHSKRSFIHDTTT
T172 KRSFIHDTTTDNVML
T173 RSFIHDTTTDNVMLR
Y220 CSLEIESYAYTEDDL
Y222 LEIESYAYTEDDLML
Y230 TEDDLMLYWKKGNDS
T327-p TTVLTMStIITGVNA
S335-p IITGVNAsMPRVSYI
Y402 GVMLDSSYSDGEVND
Y413 EVNDLGGYMPENGEK
  rat

 
S167 FFVHSKRSFIHDTTT
T172 KRSFIHDTTTDNVML
T173 RSFIHDTTTDNVMLR
Y220 CSLEIESYAYTEDDL
Y222 LEIESYAYTEDDLML
Y230 TEDDLMLYWKKGNDS
T327 TTVLTMSTIITGVNA
S335 IITGVNASMPRVSYI
Y402-p GVMLDSSySDGEVND
Y413-p EVNDLGGyMPENGEK
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