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Protein Page:
FABP7 (human)
p Phosphorylation
ac Acetylation
me Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
ub Ubiquitination
sm Sumoylation
ne Neddylation
gl O-GlcNAc
ga O-GalNAc
pa Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage
sc Succinylation

Overview
FABP7 B-FABP could be involved in the transport of a so far unknown hydrophobic ligand with potential morphogenic activity during CNS development. It is required for the establishment of the radial glial fiber system in developing brain, a system that is necessary for the migration of immature neurons to establish cortical layers. Belongs to the calycin superfamily. Fatty-acid binding protein (FABP) family. Note: This description may include information from UniProtKB.
Protein type: Cell cycle regulation; Cell development/differentiation; Lipid binding protein
Cellular Component: cell projection; cell soma; cytoplasm; nucleus
Molecular Function: transporter activity; lipid binding
Biological Process: negative regulation of cell proliferation; nervous system development; epithelial cell proliferation; neurogenesis; prepulse inhibition; transport; cell proliferation in forebrain
Reference #:  O15540 (UniProtKB)
Alt. Names/Synonyms: B-FABP; BLBP; brain lipid binding protein; Brain lipid-binding protein; Brain-type fatty acid-binding protein; DKFZp547J2313; FABP7; FABPB; fatty acid binding protein 7, brain; Fatty acid-binding protein 7; Fatty acid-binding protein, brain; Mammary-derived growth inhibitor related; mammary-derived growth inhibitor-related; MRG
Gene Symbols: FABP7
Molecular weight: 14,889 Da
Basal Isoelectric point: 5.4  Predict pI for various phosphorylation states
Protein-Specific Antibodies or siRNAs from Cell Signaling Technology® Total Proteins
Select Structure to View Below

FABP7

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 K22 QNFDEYMKALGVGFA
0 1 T54-p GDKVVIRtLStFKNt
0 1 T57-p VVIRtLStFKNtEIS
0 1 T61-p tLStFKNtEISFQLG
0 1 T117-p KDGKMVMtLtFGDVV
0 1 T119-p GKMVMtLtFGDVVAV
0 1 Y129-p DVVAVRHyEKA____
  mouse

 
K22-ub QNFDEYMkALGVGFA
T54 GGKVVIRTQCTFKNT
T57 VVIRTQCTFKNTEIN
T61 TQCTFKNTEINFQLG
T117 KDGKMVVTLTFGDIV
T119 GKMVVTLTFGDIVAV
Y129 DIVAVRCYEKA____
  rat

 
K22 QNFDEYMKALGVGFA
T54 GGKVVIRTQCTFKNT
T57 VVIRTQCTFKNTEIS
T61 TQCTFKNTEISFQLG
T117 KDGKMVVTLTFGDVV
T119 GKMVVTLTFGDVVAV
Y129 DVVAVRCYEKA____
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