Type |
Details |
Score |
Protein Domain |
Type: |
Domain |
Description: |
Sm and Sm-like proteins of the RNA-binding Lsm (like Sm) domain family arefound in all domains of life and are generally involved in important RNA-processing tasks. Lsm13-16 homologues share a domain organisation consisting ofa divergent N-terminal Lsm domain and a central or C-terminal consensus motifDFDF-x(7)-F. In few other sequences, the DFDF box is replaced by a DYDF or EFDF box [].The FFD box and TFG box are two other strongly conserved sequence motifs(Y-x-K-x(3)-FFD-x-[IL]-S and [RKH]-x(2,5)-E-x(0-2)-[RK]-x(3,4)-[DE]-TFG respectively) contained in Lsm13-15, but not Lsm16, homologues. They succeed the DFDF-x(7)-F motif and are also predicted to be of helical nature [].This entry represents the TGF box. |
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•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
124
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
157
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
305
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
240
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Greco A |
Year: |
1998 |
Journal: |
Oncogene |
Title: |
Role of the TFG N-terminus and coiled-coil domain in the transforming activity of the thyroid TRK-T3 oncogene. |
Volume: |
16 |
Issue: |
6 |
Pages: |
809-16 |
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•
•
•
•
•
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DO Term |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
462
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
385
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Albrecht M |
Year: |
2004 |
Journal: |
FEBS Lett |
Title: |
Novel Sm-like proteins with long C-terminal tails and associated methyltransferases. |
Volume: |
569 |
Issue: |
1-3 |
Pages: |
18-26 |
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•
•
•
•
•
|
Allele |
Name: |
transgene insertion IH44, GENSAT Project at Rockefeller University |
Allele Type: |
Transgenic |
Attribute String: |
Reporter |
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•
•
•
•
•
|
Strain |
Attribute String: |
mutant stock, transgenic |
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•
•
•
•
•
|
Allele |
Name: |
transgene insertion 1, Richard A Flavell |
Allele Type: |
Transgenic |
Attribute String: |
Dominant negative, Humanized sequence, Inserted expressed sequence |
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•
•
•
•
•
|
Publication |
First Author: |
Takeuchi S |
Year: |
2012 |
Journal: |
Acta Histochem Cytochem |
Title: |
Immunohistochemical Mapping of TRK-Fused Gene Products in the Rat Brainstem. |
Volume: |
45 |
Issue: |
1 |
Pages: |
57-64 |
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•
•
•
•
•
|
Publication |
First Author: |
Lim B |
Year: |
2012 |
Journal: |
Carcinogenesis |
Title: |
The TFG-TEC fusion gene created by the t(3;9) translocation in human extraskeletal myxoid chondrosarcomas encodes a more potent transcriptional activator than TEC. |
Volume: |
33 |
Issue: |
8 |
Pages: |
1450-8 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
This is the PB1 domain found in TFG protein (TRK-fused gene), an oncogenic gene product first identified as a fusion partner to nerve growth factor tyrosine kinase receptor TrkA/NTRK1 []and subsequently found as an oncogenic fusion gene in various cancers [, ]. TFG is localised at endoplasmic reticulum (ER) exit sites and modulates ER export []. It may function at the ER/ERGIC interface to locally concentrate COPII-coated transport carriers and link exit sites on the ER to ERGIC membranes []. It is also a an inhibitory regulator of the ubiquitin-proteasome system [].The PB1 domain is a modular domain mediating specific protein-protein interaction in many critical cell processes, such as osteoclastogenesis, angiogenesis, early cardiovascular development and cell polarity. A canonical PB1-PB1 interaction, which involves heterodimerization of two PB1 domains, is required for the formation of macromolecular signaling complexes ensuring specificity and fidelity during cellular signaling. The interaction between two PB1 domain depends on the type of PB1. There are three types of PB1 domains: type I which contains an OPCA motif, acidic aminoacid cluster, type II which contains a basic cluster, and type I/II which contains both an OPCA motif and a basic cluster []. The PB1 domain of TFG represent a type I/II domain. |
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•
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•
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Strain |
Attribute String: |
congenic, transgenic |
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•
•
•
•
•
|
Strain |
Attribute String: |
congenic, transgenic |
|
•
•
•
•
•
|
Publication |
First Author: |
Laouar Y |
Year: |
2005 |
Journal: |
Nat Immunol |
Title: |
Transforming growth factor-beta controls T helper type 1 cell development through regulation of natural killer cell interferon-gamma. |
Volume: |
6 |
Issue: |
6 |
Pages: |
600-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Marcoe JP |
Year: |
2012 |
Journal: |
Nat Immunol |
Title: |
TGF-β is responsible for NK cell immaturity during ontogeny and increased susceptibility to infection during mouse infancy. |
Volume: |
13 |
Issue: |
9 |
Pages: |
843-50 |
|
•
•
•
•
•
|
Publication |
First Author: |
Domingo-Gonzalez R |
Year: |
2015 |
Journal: |
Am J Physiol Lung Cell Mol Physiol |
Title: |
Transforming growth factor-β induces microRNA-29b to promote murine alveolar macrophage dysfunction after bone marrow transplantation. |
Volume: |
308 |
Issue: |
1 |
Pages: |
L86-95 |
|
•
•
•
•
•
|
Publication |
First Author: |
Domingo-Gonzalez R |
Year: |
2012 |
Journal: |
J Immunol |
Title: |
COX-2 expression is upregulated by DNA hypomethylation after hematopoietic stem cell transplantation. |
Volume: |
189 |
Issue: |
9 |
Pages: |
4528-36 |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(Itgax-TGFBR2)1Flv/? |
Background: |
C.Cg-Tg(Itgax-TGFBR2)1Flv |
Zygosity: |
ot |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
Sm and Sm-like proteins of the RNA-binding Lsm (like Sm) domain family arefound in all domains of life and are generally involved in important RNA-processing tasks. Lsm13-16 homologues share a domain organisation consisting ofa divergent N-terminal Lsm domain and a central or C-terminal consensus motifDFDF-x(7)-F. In few other sequences, the DFDF box is replaced by a DYDF or EFDF box [].The FFD box and TFG box are two other strongly conserved sequence motifs(Y-x-K-x(3)-FFD-x-[IL]-S and [RKH]-x(2,5)-E-x(0-2)-[RK]-x(3,4)-[DE]-TFG respectively) contained in Lsm13-15, but not Lsm16, homologues. They succeed the DFDF-x(7)-F motif and are also predicted to be of helical nature [].This entry represents the FFD box. |
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•
•
•
•
•
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Genotype |
Symbol: |
Eomes/? Tg(Itgax-TGFBR2)1Flv/? |
Background: |
involves: C3H * C57BL/6 * C57BL/6N |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Hsu TI |
Year: |
2015 |
Journal: |
Oncogene |
Title: |
MMP7-mediated cleavage of nucleolin at Asp255 induces MMP9 expression to promote tumor malignancy. |
Volume: |
34 |
Issue: |
7 |
Pages: |
826-37 |
|
•
•
•
•
•
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Publication |
First Author: |
Mahmood R |
Year: |
1995 |
Journal: |
Anat Embryol (Berl) |
Title: |
The effects of retinoid status on TGF beta expression during mouse embryogenesis. |
Volume: |
192 |
Issue: |
1 |
Pages: |
21-33 |
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•
•
•
•
•
|
Publication |
First Author: |
Hanks BA |
Year: |
2013 |
Journal: |
J Clin Invest |
Title: |
Type III TGF-β receptor downregulation generates an immunotolerant tumor microenvironment. |
Volume: |
123 |
Issue: |
9 |
Pages: |
3925-40 |
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•
•
•
•
•
|
Publication |
First Author: |
Laouar Y |
Year: |
2008 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
TGF-beta signaling in dendritic cells is a prerequisite for the control of autoimmune encephalomyelitis. |
Volume: |
105 |
Issue: |
31 |
Pages: |
10865-70 |
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•
•
•
•
•
|
Publication |
First Author: |
Mondanelli G |
Year: |
2017 |
Journal: |
Immunity |
Title: |
A Relay Pathway between Arginine and Tryptophan Metabolism Confers Immunosuppressive Properties on Dendritic Cells. |
Volume: |
46 |
Issue: |
2 |
Pages: |
233-244 |
|
•
•
•
•
•
|
Publication |
First Author: |
Allen SJ |
Year: |
2011 |
Journal: |
J Virol |
Title: |
Adaptive and innate transforming growth factor beta signaling impact herpes simplex virus 1 latency and reactivation. |
Volume: |
85 |
Issue: |
21 |
Pages: |
11448-56 |
|
•
•
•
•
•
|
Publication |
First Author: |
Coomes SM |
Year: |
2011 |
Journal: |
Am J Pathol |
Title: |
Severe gammaherpesvirus-induced pneumonitis and fibrosis in syngeneic bone marrow transplant mice is related to effects of transforming growth factor-β. |
Volume: |
179 |
Issue: |
5 |
Pages: |
2382-96 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tritschler F |
Year: |
2009 |
Journal: |
Mol Cell |
Title: |
Structural basis for the mutually exclusive anchoring of P body components EDC3 and Tral to the DEAD box protein DDX6/Me31B. |
Volume: |
33 |
Issue: |
5 |
Pages: |
661-8 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
Sm and Sm-like proteins of the RNA-binding Lsm (like Sm) domain family arefound in all domains of life and are generally involved in important RNA-processing tasks. Lsm13-16 homologs share a domain organisation consisting ofa divergent N-terminal Lsm domain and a central or C-terminal consensus motifDFDF-x(7)-F closely preceded and followed by further phenylalanines andcharged aspartates/glutamates and arginines/lysines/histidines. The variableseven-residue tract of this consensus motif usually contains an asparagine atthe third or fourth position except of one sequence where the asparagine isreplaced by a glycine. In few other sequences, the DFDF box is replaced by aDYDF or EFDF box []. The DFDF domain is a heterodimerization domain, whichadopts a helical conformation upon binding. It folds into twoconsecutive alpha helices that are preceded and connected by the FDF and arelated FDK sequence [].Two other strongly conserved FFD box and TFG box sequence motifs Y-x-K-x(3)-FFD-x-[IL]-S and [RKH]-x(2,5)-E-x(0-2)-[RK]-x(3,4)-[DE]-TFG contained inLsm13-15, but not Lsm16, homologs succeed the DFDF-x(7)-F motif and are alsopredicted to be of helical nature [].This entry represents the DFDF domain. |
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•
•
•
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•
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Publication |
First Author: |
Hirose S |
Year: |
2023 |
Journal: |
Front Immunol |
Title: |
IL-17A expression by both T cells and non-T cells contribute to HSV-IL-2-induced CNS demyelination. |
Volume: |
14 |
|
Pages: |
1102486 |
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•
•
•
•
•
|
Publication |
First Author: |
Daussy C |
Year: |
2014 |
Journal: |
J Exp Med |
Title: |
T-bet and Eomes instruct the development of two distinct natural killer cell lineages in the liver and in the bone marrow. |
Volume: |
211 |
Issue: |
3 |
Pages: |
563-77 |
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•
•
•
•
•
|
Publication |
First Author: |
Sanjabi S |
Year: |
2009 |
Journal: |
Immunity |
Title: |
Opposing effects of TGF-beta and IL-15 cytokines control the number of short-lived effector CD8+ T cells. |
Volume: |
31 |
Issue: |
1 |
Pages: |
131-44 |
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•
•
•
•
•
|
Publication |
First Author: |
Wong WW |
Year: |
2014 |
Journal: |
Blood |
Title: |
cIAPs and XIAP regulate myelopoiesis through cytokine production in an RIPK1- and RIPK3-dependent manner. |
Volume: |
123 |
Issue: |
16 |
Pages: |
2562-72 |
|
•
•
•
•
•
|
Publication |
First Author: |
Town T |
Year: |
2008 |
Journal: |
Nat Med |
Title: |
Blocking TGF-beta-Smad2/3 innate immune signaling mitigates Alzheimer-like pathology. |
Volume: |
14 |
Issue: |
6 |
Pages: |
681-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sumimoto H |
Year: |
2007 |
Journal: |
Sci STKE |
Title: |
Structure and function of the PB1 domain, a protein interaction module conserved in animals, fungi, amoebas, and plants. |
Volume: |
2007 |
Issue: |
401 |
Pages: |
re6 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
287
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
508
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
508
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
The Gene Expression Nervous System Atlas (GENSAT) Project, The Rockefeller University (New York, NY) |
Year: |
2005 |
Journal: |
Database Download |
Title: |
MGI download of GENSAT transgene data |
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•
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