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Protein Page:
DJ-1 (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
DJ-1 associated with autosomal recessive early onset parkinsonism. Involved in the oxidative stress response. Three cysteines in DJ-1 may be oxidized to cysteine sulphonic acid in the cellular response to H2O2. Loss of DJ-1 function may lead to neurodegeneration. Note: This description may include information from UniProtKB.
Protein type: Transcription regulation; Oncoprotein; EC 3.4.-.-; Nuclear receptor co-regulator
Cellular Component: mitochondrion; axon; cytoplasm; nucleus; cytosol
Molecular Function: peptidase activity; mRNA binding; protein binding; protein homodimerization activity; peroxidase activity; peroxiredoxin activity
Biological Process: cell death; response to drug; mitochondrion organization and biogenesis; protein stabilization; adult locomotory behavior; membrane hyperpolarization; proteolysis; membrane depolarization; single fertilization; regulation of neuron apoptosis; regulation of inflammatory response; hydrogen peroxide metabolic process; autophagy; dopamine uptake; negative regulation of neuron apoptosis; inflammatory response; negative regulation of protein binding
Reference #:  Q99497 (UniProtKB)
Alt. Names/Synonyms: DJ-1; DJ1; FLJ27376; FLJ34360; FLJ92274; Oncogene DJ1; PARK7; Parkinson disease (autosomal recessive, early onset) 7; Parkinson disease protein 7; Protein DJ-1
Gene Symbols: PARK7
Molecular weight: 19,891 Da
Basal Isoelectric point: 6.33  Predict pI for various phosphorylation states
CST Pathways:  Parkinson's Disease
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
Select Structure to View Below

DJ-1

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 3 K41-u TVAGLAGkDPVQCSR
0 1 T19-p KGAEEMEtVIPVDVM
0 1 K32 VMRRAGIKVTVAGLA
0 1 S47 GkDPVQCSRDVVICP
0 12 K62-a DASLEDAkkEGPyDV
0 1 K63-a ASLEDAkkEGPyDVV
0 16 Y67-p DAkkEGPyDVVVLPG
4 0 K130-s VTTHPLAkDKMMNGG
0 1 K132 THPLAkDKMMNGGHy
0 3 Y139-p KMMNGGHytysENRV
0 2 T140-p MMNGGHytysENRVE
0 2 Y141-p MNGGHytysENRVEk
0 1 S142-p NGGHytysENRVEkD
0 2 K148-a ysENRVEkDGLILTS
0 2 K148-u ysENRVEkDGLILTS
1 1 T154 EkDGLILTSRGPGTS
1 1 S155 kDGLILTSRGPGTSF
0 2 K175-u IVEALNGkEVAAQVK
0 1 K182 kEVAAQVKAPLVLkD
0 1 K188-u VKAPLVLkD______
  mouse

 
K41-u TVAGLAGkDPVQCsR
T19 KGAEEMETVIPVDVM
K32-u VMRRAGIkVTVAGLA
S47-p GkDPVQCsRDVMICP
K62 DTSLEDAKTQGPYDV
T63 TSLEDAKTQGPYDVV
Y67 DAKTQGPYDVVVLPG
K130 VTTHPLAKDkMMNGS
K132-u THPLAKDkMMNGSHY
Y139 kMMNGSHYsYsESRV
S140-p MMNGSHYsYsESRVE
Y141 MNGSHYsYsESRVEk
S142-p NGSHYsYsESRVEkD
K148-a YsESRVEkDGLILTS
K148-u YsESRVEkDGLILTS
T154 EkDGLILTSRGPGTS
S155 kDGLILTSRGPGTSF
K175 IVEALVGKDMANQVk
K182-u KDMANQVkAPLVLKD
K188 VkAPLVLKD______
  rat

 
K41 TVAGLAGKDPVQCSR
T19 KGAEEMETVIPVDIM
K32 IMRRAGIKVTVAGLA
S47 GKDPVQCSRDVVICP
K62 DTSLEEAKTQGPYDV
T63 TSLEEAKTQGPYDVV
Y67 EAKTQGPYDVVVLPG
K130 VTSHPLAKDKMMNGS
K132 SHPLAKDKMMNGSHY
Y139 KMMNGSHYSYSESRV
S140 MMNGSHYSYSESRVE
Y141 MNGSHYSYSESRVEK
S142 NGSHYSYSESRVEKD
K148 YSESRVEKDGLILts
K148 YSESRVEKDGLILts
T154-p EKDGLILtsRGPGTS
S155-p KDGLILtsRGPGTSF
K175 IVEALSGKDMANQVK
K182 KDMANQVKAPLVLKD
K188 VKAPLVLKD______
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