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Protein Page:
VAMP3 (human)
p Phosphorylation
a Acetylation
m Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
u Ubiquitination
s Sumoylation
n Neddylation
gl O-GlcNAc
ga O-GalNAc
h Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage

Overview
VAMP3 SNARE involved in vesicular transport from the late endosomes to the trans-Golgi network. Belongs to the synaptobrevin family. Note: This description may include information from UniProtKB.
Protein type: Membrane protein, integral
Cellular Component: SNARE complex; recycling endosome; synaptic vesicle; neuron projection; clathrin-coated vesicle; apical plasma membrane; integral to membrane; plasma membrane; clathrin coated vesicle membrane; cell junction; secretory granule
Molecular Function: SNAP receptor activity; protein binding; SNARE binding; syntaxin-1 binding
Biological Process: vesicle-mediated transport; vesicle fusion; exocytosis; neurotransmitter secretion; Golgi to plasma membrane protein transport; protein complex assembly; positive regulation of receptor recycling; retrograde transport, endosome to Golgi; vesicle docking during exocytosis; calcium ion-dependent exocytosis
Reference #:  Q15836 (UniProtKB)
Alt. Names/Synonyms: CEB; Cellubrevin; SYB3; Synaptobrevin-3; VAMP-3; VAMP3; Vesicle-associated membrane protein 3; vesicle-associated membrane protein 3 (cellubrevin)
Gene Symbols: VAMP3
Molecular weight: 11,309 Da
Basal Isoelectric point: 8.89  Predict pI for various phosphorylation states
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
Select Structure to View Below

VAMP3

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 T6 __MSTGPTAATGsNR
0 3 S11-p GPTAATGsNRRLQQT
0 92 K35-u IMRVNVDkVLERDQk
0 89 K42-u kVLERDQkLsELDDR
0 20 S44-p LERDQkLsELDDRAD
0 36 S58-p DALQAGAsQFETsAA
0 7 S63-p GAsQFETsAAkLkRK
0 16 K66-u QFETsAAkLkRKYWW
0 5 K68-u ETsAAkLkRKYWWKN
  mouse

 
S10-p TGVPSGSsAATGsNR
S15-p GSsAATGsNRRLQQT
K39-u IMRVNVDkVLERDQk
K46-u kVLERDQkLsELDDR
S48-p LERDQkLsELDDRAD
S62-p DALQAGAsQFETsAA
S67-p GAsQFETsAAkLKRK
K70-u QFETsAAkLKRKYWW
K72 ETsAAkLKRKYWWKN
  rat

 
S10 TGVPSGSSAATGSNR
S15 GSSAATGSNRRLQQT
K39 IMRVNVDKVLERDQK
K46 KVLERDQKLSELDDR
S48 LERDQKLSELDDRAD
S62 DALQAGASQFETSAA
S67 GASQFETSAAKLKRK
K70 QFETSAAKLKRKYWW
K72 ETSAAKLKRKYWWKN
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