Homo sapiens Protein: PDGFC
Summary
InnateDB Protein IDBP-379210.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PDGFC
Protein Name platelet derived growth factor C
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000410048
InnateDB Gene IDBG-42546 (PDGFC)
Protein Structure
UniProt Annotation
Function Growth factor that plays an essential role in the regulation of embryonic development, cell proliferation, cell migration, survival and chemotaxis. Potent mitogen and chemoattractant for cells of mesenchymal origin. Required for normal skeleton formation during embryonic development, especially for normal development of the craniofacial skeleton and for normal development of the palate. Required for normal skin morphogenesis during embryonic development. Plays an important role in wound healing, where it appears to be involved in three stages: inflammation, proliferation and remodeling. Plays an important role in angiogenesis and blood vessel development. Involved in fibrotic processes, in which transformation of interstitial fibroblasts into myofibroblasts plus collagen deposition occurs. The CUB domain has mitogenic activity in coronary artery smooth muscle cells, suggesting a role beyond the maintenance of the latency of the PDGF domain. In the nucleus, PDGFC seems to have additional function. {ECO:0000269PubMed:10806482, ECO:0000269PubMed:10858496, ECO:0000269PubMed:11297552, ECO:0000269PubMed:11854040, ECO:0000269PubMed:12032822, ECO:0000269PubMed:15061151, ECO:0000269PubMed:15372073, ECO:0000269PubMed:15389578, ECO:0000269PubMed:15728360, ECO:0000269PubMed:15911618, ECO:0000269PubMed:16439802, ECO:0000269PubMed:18055825}.
Subcellular Localization Cytoplasm. Secreted. Nucleus. Cytoplasmic granule. Note=Sumoylated form is predominant in the nucleus. Stored in alpha granules in platelets. Membrane associated when bound to receptors.
Disease Associations
Tissue Specificity Expressed in the fallopian tube, vascular smooth muscle cells in kidney, breast and colon and in visceral smooth muscle of the gastrointestinal tract. Highly expressed in retinal pigment epithelia. Expressed in medulloblastoma. In the kidney, constitutively expressed in parietal epithelial cells of Bowman's capsule, tubular epithelial cells and in arterial endothelial cells (at protein level). Highly expressed in the platelets, prostate, testis and uterus. Higher expression is observed in uterine leiomyomata. Weaker expression in the spleen, thymus, heart, pancreas, liver, ovary cells and small intestine, and negligible expression in the colon and peripheral blood leukocytes. {ECO:0000269PubMed:10806482, ECO:0000269PubMed:11004490, ECO:0000269PubMed:11297552, ECO:0000269PubMed:11342471, ECO:0000269PubMed:11854040, ECO:0000269PubMed:12176024, ECO:0000269PubMed:15061151, ECO:0000269PubMed:17482170, ECO:0000269PubMed:18055825}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
Experimentally validated
Total 9 [view]
Protein-Protein 8 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005161 platelet-derived growth factor receptor binding
GO:0005515 protein binding
GO:0008083 growth factor activity
GO:0042803 protein homodimerization activity
Biological Process
GO:0007417 central nervous system development
GO:0045740 positive regulation of DNA replication
GO:0048008 platelet-derived growth factor receptor signaling pathway
GO:0048146 positive regulation of fibroblast proliferation
GO:0051781 positive regulation of cell division
Cellular Component
GO:0000139 Golgi membrane
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005788 endoplasmic reticulum lumen
GO:0005886 plasma membrane
GO:0009986 cell surface
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR000859 CUB domain
IPR029034 Cystine-knot cytokine
PFAM PF00431
PRINTS
PIRSF
SMART SM00042
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9NRA1
PhosphoSite PhosphoSite-Q9NRA1
TrEMBL
UniProt Splice Variant
Entrez Gene 56034
UniGene Hs.600482
RefSeq
HUGO HGNC:8801
OMIM 608452
CCDS
HPRD 10529
IMGT
EMBL AB033831 AC092608 AC093325 AF091434 AF244813 AF260738 AK300480 AM922296 AY358493 BC136662 CH471056
GenPept AAF00049 AAF80597 AAI36663 AAK51637 AAQ88857 AAY40906 BAB03266 BAG62196 CAP58278 EAX04874 EAX04875