Version 5.4
Bos taurus Protein: ENG
Summary
InnateDB Protein IDBP-691180.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ENG
Protein Name endoglin
Synonyms
Species Bos taurus
Ensembl Protein ENSBTAP00000048579
InnateDB Gene IDBG-639059 (ENG)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005024 transforming growth factor beta-activated receptor activity
GO:0005072 transforming growth factor beta receptor, cytoplasmic mediator activity
GO:0005114 type II transforming growth factor beta receptor binding
GO:0005515 protein binding
GO:0005534 galactose binding
GO:0005539 glycosaminoglycan binding
GO:0034713 type I transforming growth factor beta receptor binding
GO:0042803 protein homodimerization activity
GO:0050431 transforming growth factor beta binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001300 chronological cell aging
GO:0001525 angiogenesis
GO:0001569 patterning of blood vessels
GO:0001570 vasculogenesis
GO:0001666 response to hypoxia
GO:0001934 positive regulation of protein phosphorylation
GO:0001937 negative regulation of endothelial cell proliferation
GO:0001947 heart looping
GO:0003084 positive regulation of systemic arterial blood pressure
GO:0003273 cell migration involved in endocardial cushion formation
GO:0006355 regulation of transcription, DNA-templated
GO:0007179 transforming growth factor beta receptor signaling pathway
GO:0007507 heart development
GO:0010862 positive regulation of pathway-restricted SMAD protein phosphorylation
GO:0016477 cell migration
GO:0017015 regulation of transforming growth factor beta receptor signaling pathway
GO:0022009 central nervous system vasculogenesis
GO:0022617 extracellular matrix disassembly
GO:0030336 negative regulation of cell migration
GO:0030513 positive regulation of BMP signaling pathway
GO:0031953 negative regulation of protein autophosphorylation
GO:0035556 intracellular signal transduction
GO:0042060 wound healing
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0048745 smooth muscle tissue development
GO:0048844 artery morphogenesis
GO:0048845 venous blood vessel morphogenesis
GO:0048870 cell motility
GO:0051001 negative regulation of nitric-oxide synthase activity
GO:0060326 cell chemotaxis
GO:0060394 negative regulation of pathway-restricted SMAD protein phosphorylation
GO:0070483 detection of hypoxia
Cellular Component
GO:0005615 extracellular space
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0009897 external side of plasma membrane
GO:0009986 cell surface
GO:0072563 endothelial microparticle
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt
PhosphoSite PhosphoSite-
TrEMBL Q1RMV1
UniProt Splice Variant
Entrez Gene 615844
UniGene Bt.5220
RefSeq NP_001069865
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC114687 DAAA02032163 DAAA02032164 DAAA02032165
GenPept AAI14688

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca