Homo sapiens Protein: TGFBR1
Summary
InnateDB Protein IDBP-589188.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TGFBR1
Protein Name transforming growth factor, beta receptor 1
Synonyms AAT5; ACVRLK4; ALK-5; ALK5; ESS1; LDS1; LDS1A; LDS2A; MSSE; SKR4; TGFR-1;
Species Homo sapiens
Ensembl Protein ENSP00000447297
InnateDB Gene IDBG-78488 (TGFBR1)
Protein Structure
UniProt Annotation
Function Transmembrane serine/threonine kinase forming with the TGF-beta type II serine/threonine kinase receptor, TGFBR2, the non-promiscuous receptor for the TGF-beta cytokines TGFB1, TGFB2 and TGFB3. Transduces the TGFB1, TGFB2 and TGFB3 signal from the cell surface to the cytoplasm and is thus regulating a plethora of physiological and pathological processes including cell cycle arrest in epithelial and hematopoietic cells, control of mesenchymal cell proliferation and differentiation, wound healing, extracellular matrix production, immunosuppression and carcinogenesis. The formation of the receptor complex composed of 2 TGFBR1 and 2 TGFBR2 molecules symmetrically bound to the cytokine dimer results in the phosphorylation and the activation of TGFBR1 by the constitutively active TGFBR2. Activated TGFBR1 phosphorylates SMAD2 which dissociates from the receptor and interacts with SMAD4. The SMAD2-SMAD4 complex is subsequently translocated to the nucleus where it modulates the transcription of the TGF-beta-regulated genes. This constitutes the canonical SMAD-dependent TGF-beta signaling cascade. Also involved in non- canonical, SMAD-independent TGF-beta signaling pathways. For instance, TGFBR1 induces TRAF6 autoubiquitination which in turn results in MAP3K7 ubiquitination and activation to trigger apoptosis. Also regulates epithelial to mesenchymal transition through a SMAD-independent signaling pathway through PARD6A phosphorylation and activation. {ECO:0000269PubMed:15761148, ECO:0000269PubMed:16754747, ECO:0000269PubMed:18758450, ECO:0000269PubMed:7774578, ECO:0000269PubMed:8752209, ECO:0000269PubMed:8980228, ECO:0000269PubMed:9346908}.
Subcellular Localization Cell membrane; Single-pass type I membrane protein. Cell junction, tight junction.
Disease Associations Loeys-Dietz syndrome 1 (LDS1) [MIM:609192]: An aortic aneurysm syndrome with widespread systemic involvement, characterized by arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate. Physical findings include prominent joint laxity, easy bruising, wide and atrophic scars, velvety and translucent skin with easily visible veins, spontaneous rupture of the spleen or bowel, and catastrophic complications of pregnancy, including rupture of the gravid uterus and the arteries, either during pregnancy or in the immediate postpartum period. Some patients have craniosynostosis, exotropy, micrognathia and retrognathia, structural brain abnormalities, and intellectual deficit. {ECO:0000269PubMed:15731757, ECO:0000269PubMed:16596670, ECO:0000269PubMed:16791849, ECO:0000269PubMed:16928994, ECO:0000269PubMed:19883511, ECO:0000269PubMed:22113417}. Note=The disease is caused by mutations affecting the gene represented in this entry. TGFBR1 mutation Gln-487 has been reported to be associated with thoracic aortic aneurysms and dissection (TAAD) (PubMed:16791849). This phenotype, also known as thoracic aortic aneurysms type 5 (AAT5), is distinguised from LDS1 by having aneurysms restricted to thoracic aorta. It is unclear, however, if this condition is fulfilled in individuals bearing Gln-487 mutation, that is why they are considered as LDS1 by the OMIM resource. {ECO:0000269PubMed:16791849}.Multiple self-healing squamous epithelioma (MSSE) [MIM:132800]: A disorder characterized by multiple skin tumors that undergo spontaneous regression. Tumors appear most often on sun-exposed regions, are locally invasive, and undergo spontaneous resolution over a period of months leaving pitted scars. {ECO:0000269PubMed:21358634}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Found in all tissues examined, most abundant in placenta and least abundant in brain and heart.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 369 experimentally validated interaction(s) in this database.
They are also associated with 18 interaction(s) predicted by orthology.
Experimentally validated
Total 369 [view]
Protein-Protein 366 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 1 [view]
RNA-RNA 1 [view]
DNA-RNA 0
Predicted by orthology
Total 18 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004672 protein kinase activity
GO:0004674 protein serine/threonine kinase activity
GO:0004675 transmembrane receptor protein serine/threonine kinase activity
GO:0004702 receptor signaling protein serine/threonine kinase activity
GO:0004713 protein tyrosine kinase activity
GO:0005024 transforming growth factor beta-activated receptor activity
GO:0005025 transforming growth factor beta receptor activity, type I
GO:0005114 type II transforming growth factor beta receptor binding
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016772 transferase activity, transferring phosphorus-containing groups
GO:0019838 growth factor binding
GO:0046332 SMAD binding
GO:0046872 metal ion binding
GO:0050431 transforming growth factor beta binding
GO:0070411 I-SMAD binding
Biological Process
GO:0000186 activation of MAPKK activity
GO:0001501 skeletal system development
GO:0001701 in utero embryonic development
GO:0001822 kidney development
GO:0001837 epithelial to mesenchymal transition
GO:0006355 regulation of transcription, DNA-templated
GO:0006468 protein phosphorylation
GO:0006915 apoptotic process
GO:0007050 cell cycle arrest
GO:0007165 signal transduction
GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
GO:0007179 transforming growth factor beta receptor signaling pathway
GO:0007507 heart development
GO:0008284 positive regulation of cell proliferation
GO:0008354 germ cell migration
GO:0009952 anterior/posterior pattern specification
GO:0010862 positive regulation of pathway-restricted SMAD protein phosphorylation
GO:0018105 peptidyl-serine phosphorylation
GO:0018107 peptidyl-threonine phosphorylation
GO:0023014 signal transduction by phosphorylation
GO:0030199 collagen fibril organization
GO:0030307 positive regulation of cell growth
GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
GO:0031396 regulation of protein ubiquitination
GO:0032331 negative regulation of chondrocyte differentiation
GO:0042060 wound healing
GO:0043062 extracellular structure organization
GO:0045893 positive regulation of transcription, DNA-templated
GO:0048538 thymus development
GO:0048663 neuron fate commitment
GO:0048701 embryonic cranial skeleton morphogenesis
GO:0048705 skeletal system morphogenesis
GO:0048762 mesenchymal cell differentiation
GO:0048844 artery morphogenesis
GO:0048870 cell motility
GO:0051272 positive regulation of cellular component movement
GO:0051897 positive regulation of protein kinase B signaling
GO:0060017 parathyroid gland development
GO:0060021 palate development
GO:0060037 pharyngeal system development
GO:0060389 pathway-restricted SMAD protein phosphorylation
GO:0060391 positive regulation of SMAD protein import into nucleus
GO:0070723 response to cholesterol
GO:0071560 cellular response to transforming growth factor beta stimulus
GO:2001235 positive regulation of apoptotic signaling pathway
GO:2001237 negative regulation of extrinsic apoptotic signaling pathway
Cellular Component
GO:0005886 plasma membrane
GO:0005923 tight junction
GO:0016020 membrane
GO:0043235 receptor complex
GO:0070022 transforming growth factor beta receptor homodimeric complex
Protein Structure and Domains
PDB ID
InterPro IPR000472 TGF-beta receptor/activin receptor, type I/II
IPR000719 Protein kinase domain
IPR001245 Serine-threonine/tyrosine-protein kinase catalytic domain
IPR002290 Serine/threonine/dual specificity protein kinase, catalytic domain
IPR003605 TGF beta receptor, GS motif
IPR011009 Protein kinase-like domain
IPR020635 Tyrosine-protein kinase, catalytic domain
PFAM PF01064
PF00069
PF07714
PF08515
PRINTS PR00109
PIRSF
SMART SM00220
SM00467
SM00219
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P36897
PhosphoSite PhosphoSite-P36897
TrEMBL F8W0K6
UniProt Splice Variant
Entrez Gene 7046
UniGene Hs.625128
RefSeq
HUGO HGNC:11772
OMIM 190181
CCDS
HPRD 01822
IMGT
EMBL AF035662 AF035663 AF035664 AF035665 AF035666 AF035667 AF035668 AF035669 AF035670 AF054590 AF054591 AF054592 AF054593 AF054594 AF054595 AF054596 AF054597 AF054598 AJ619019 AJ619020 AL162427 AY497473 BC071181 L11695
GenPept AAA16073 AAC08998 AAD02042 AAH71181 AAR32097 CAF02096 CAF02097