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Protein Page:
GAD67 (human)
p Phosphorylation
a Acetylation
m Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
u Ubiquitination
s Sumoylation
n Neddylation
g O-GlcNAc
h Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage

Overview
GAD67 Catalyzes the production of GABA. Homodimer. Isoform 3 is expressed in pancreatic islets, testis, adrenal cortex, and perhaps other endocrine tissues, but not in brain. Belongs to the group II decarboxylase family. 3 isoforms of the human protein are produced by alternative splicing. Note: This description may include information from UniProtKB.
Protein type: Carbohydrate Metabolism - butanoate; Amino Acid Metabolism - alanine, aspartate and glutamate; Mitochondrial; Lyase; EC 4.1.1.15; Other Amino Acids Metabolism - taurine and hypotaurine; Other Amino Acids Metabolism - beta-alanine
Cellular Component: plasma membrane; intracellular; vesicle membrane
Molecular Function: protein binding; glutamate decarboxylase activity; pyridoxal phosphate binding
Biological Process: response to drug; glutamate catabolic process; synaptic transmission; glutamate decarboxylation to succinate; neurotransmitter secretion; protein-pyridoxal-5-phosphate linkage; neurotransmitter biosynthetic process
Reference #:  Q99259 (UniProtKB)
Alt. Names/Synonyms: 67 kDa glutamic acid decarboxylase; DCE1; FLJ45882; GAD; GAD-67; GAD1; GAD67; Glutamate decarboxylase 1; glutamate decarboxylase 1 (brain, 67kDa); Glutamate decarboxylase 67 kDa isoform; SCP
Gene Symbols: GAD1
Molecular weight: 66,897 Da
Basal Isoelectric point: 7.54  Predict pI for various phosphorylation states
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
Select Structure to View Below

GAD67

Protein Structure Not Found.


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Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

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 S56 GFLQRTNSLEEKSRL
0 1 K60 RTNSLEEKSRLVSAF
0 2 S72 SAFKERQSsKNLLSC
0 3 S73-p AFKERQSsKNLLSCE
0 4 K74 FKERQSsKNLLSCEN
0 6 S78 QSsKNLLSCENSDRD
1 0 T91-p RDARFRRtETDFSNL
0 35 Y265-p YSIMAARyKYFPEVK
0 1 K471 FWLMWKAKGTVGFEN
0 1 S571-p NFFRMVIsNPAATQS
  mouse

 
S55-p GFLQRTNsLEEKSRL
K59 RTNsLEEKSRLVSAF
S71-p SAFRERQssKNLLsC
S72-p AFRERQssKNLLsCE
K73 FRERQssKNLLsCEN
S77-p QssKNLLsCENSDQG
T90 QGARFRRTETDFSNL
Y264 YSIMAARYKYFPEVK
K470-u FWLMWKAkGTVGFEN
S570 NFFRMVISNPAATQS
  rat

 
S55 GFLQRTNSLEEkSRL
K59-u RTNSLEEkSRLVSAF
A71 SAFRERQASkNLLSC
S72 AFRERQASkNLLSCE
K73-u FRERQASkNLLSCEN
S77 QASkNLLSCENSDPG
T90 PGARFRRTETDFSNL
Y264-p YSIMAARyKYFPEVK
K470 FWLMWKAKGTVGFEN
S570 NFFRMVISNPAATQS
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