Homo sapiens Protein: GPC1
Summary
InnateDB Protein IDBP-84687.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GPC1
Protein Name glypican 1
Synonyms glypican;
Species Homo sapiens
Ensembl Protein ENSP00000264039
InnateDB Gene IDBG-84685 (GPC1)
Protein Structure
UniProt Annotation
Function Cell surface proteoglycan that bears heparan sulfate. Binds, via the heparan sulfate side chains, alpha-4 (V) collagen and participates in Schwann cell myelination (By similarity). May act as a catalyst in increasing the rate of conversion of prion protein PRPN(C) to PRNP(Sc) via associating (via the heparan sulfate side chains) with both forms of PRPN, targeting them to lipid rafts and facilitating their interaction. Required for proper skeletal muscle differentiation by sequestering FGF2 in lipid rafts preventing its binding to receptors (FGFRs) and inhibiting the FGF-mediated signaling. {ECO:0000250, ECO:0000269PubMed:19936054, ECO:0000269PubMed:21642435}.
Subcellular Localization Cell membrane; Lipid-anchor, GPI-anchor; Extracellular side. Endosome. Note=S-nitrosylated form recycled in endosomes. Localizes to CAV1-containing vesicles close to the cell surface. Cleavage of heparan sulfate side chains takes place mainly in late endosomes. Associates with both forms of PRNP in lipid rafts. Colocalizes with APP in perinuclear compartments and with CP in intracellular compartments. Associates with fibrillar APP Abeta peptides in lipid rafts in Alzheimer disease brains.Secreted glypican-1: Secreted, extracellular space.
Disease Associations Note=Associates (via the heparan sulfate side chains) with fibrillar APP-beta amyloid peptides in primitive and classic amyloid plaques and may be involved in the deposition of these senile plaques in the Alzheimer disease (AD) brain.Note=Misprocessing of GPC1 is found in fibroblasts of patients with Niemann-Pick Type C1 disease. This is due to the defective deaminative degradation of heparan sulfate chains.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
Experimentally validated
Total 7 [view]
Protein-Protein 7 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005507 copper ion binding
GO:0017134 fibroblast growth factor binding
GO:0043236 laminin binding
GO:0043395 heparan sulfate proteoglycan binding
Biological Process
GO:0001523 retinoid metabolic process
GO:0005975 carbohydrate metabolic process
GO:0006024 glycosaminoglycan biosynthetic process
GO:0006027 glycosaminoglycan catabolic process
GO:0007411 axon guidance
GO:0007603 phototransduction, visible light
GO:0014037 Schwann cell differentiation
GO:0030200 heparan sulfate proteoglycan catabolic process
GO:0030203 glycosaminoglycan metabolic process
GO:0030204 chondroitin sulfate metabolic process
GO:0032288 myelin assembly
GO:0040037 negative regulation of fibroblast growth factor receptor signaling pathway
GO:0044281 small molecule metabolic process
GO:2001016 positive regulation of skeletal muscle cell differentiation
Cellular Component
GO:0005578 proteinaceous extracellular matrix
GO:0005615 extracellular space
GO:0005768 endosome
GO:0005796 Golgi lumen
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0016020 membrane
GO:0031225 anchored component of membrane
GO:0043202 lysosomal lumen
GO:0045121 membrane raft
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR001863 Glypican
PFAM PF01153
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P35052
PhosphoSite PhosphoSite-P35052
TrEMBL
UniProt Splice Variant
Entrez Gene 2817
UniGene Hs.328232
RefSeq NP_002072
HUGO HGNC:4449
OMIM 600395
CCDS CCDS2534
HPRD 02671
IMGT
EMBL AC110619 AK095397 AK096638 BC051279 CH471063 X54232
GenPept AAH51279 AAY24160 BAG53043 BAG53345 CAA38139 EAW71180 EAW71183