Type |
Details |
Score |
Publication |
First Author: |
Birk OS |
Year: |
2000 |
Journal: |
Nature |
Title: |
The LIM homeobox gene Lhx9 is essential for mouse gonad formation. |
Volume: |
403 |
Issue: |
6772 |
Pages: |
909-13 |
|
•
•
•
•
•
|
Publication |
First Author: |
Buaas FW |
Year: |
2009 |
Journal: |
Hum Mol Genet |
Title: |
The transcription co-factor CITED2 functions during sex determination and early gonad development. |
Volume: |
18 |
Issue: |
16 |
Pages: |
2989-3001 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhou D |
Year: |
2001 |
Journal: |
Nucleic Acids Res |
Title: |
PNRC2 is a 16 kDa coactivator that interacts with nuclear receptors through an SH3-binding motif. |
Volume: |
29 |
Issue: |
19 |
Pages: |
3939-48 |
|
•
•
•
•
•
|
Publication |
First Author: |
Manceau V |
Year: |
2008 |
Journal: |
J Mol Biol |
Title: |
Different requirements of the kinase and UHM domains of KIS for its nuclear localization and binding to splicing factors. |
Volume: |
381 |
Issue: |
3 |
Pages: |
748-62 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kaneko K |
Year: |
2021 |
Journal: |
JCI Insight |
Title: |
Rap1 in the VMH regulates glucose homeostasis. |
Volume: |
6 |
Issue: |
11 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Ellsworth BS |
Year: |
2006 |
Journal: |
Mol Endocrinol |
Title: |
FOXL2 in the pituitary: molecular, genetic, and developmental analysis. |
Volume: |
20 |
Issue: |
11 |
Pages: |
2796-805 |
|
•
•
•
•
•
|
Publication |
First Author: |
McNay DE |
Year: |
2006 |
Journal: |
Mol Endocrinol |
Title: |
Mash1 is required for generic and subtype differentiation of hypothalamic neuroendocrine cells. |
Volume: |
20 |
Issue: |
7 |
Pages: |
1623-32 |
|
•
•
•
•
•
|
Publication |
First Author: |
Knoll JG |
Year: |
2013 |
Journal: |
Front Endocrinol (Lausanne) |
Title: |
Developmental profile and sexually dimorphic expression of kiss1 and kiss1r in the fetal mouse brain. |
Volume: |
4 |
|
Pages: |
140 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ludbrook LM |
Year: |
2012 |
Journal: |
Endocrinology |
Title: |
Excess DAX1 leads to XY ovotesticular disorder of sex development (DSD) in mice by inhibiting steroidogenic factor-1 (SF1) activation of the testis enhancer of SRY-box-9 (Sox9). |
Volume: |
153 |
Issue: |
4 |
Pages: |
1948-58 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wainwright EN |
Year: |
2013 |
Journal: |
Biol Reprod |
Title: |
SOX9 regulates microRNA miR-202-5p/3p expression during mouse testis differentiation. |
Volume: |
89 |
Issue: |
2 |
Pages: |
34 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mohan DR |
Year: |
2023 |
Journal: |
Cancer Res |
Title: |
β-Catenin-Driven Differentiation Is a Tissue-Specific Epigenetic Vulnerability in Adrenal Cancer. |
Volume: |
83 |
Issue: |
13 |
Pages: |
2123-2141 |
|
•
•
•
•
•
|
Publication |
First Author: |
Haraguchi H |
Year: |
2019 |
Journal: |
FASEB J |
Title: |
Mdm2-p53-SF1 pathway in ovarian granulosa cells directs ovulation and fertilization by conditioning oocyte quality. |
Volume: |
33 |
Issue: |
2 |
Pages: |
2610-2620 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pelling M |
Year: |
2011 |
Journal: |
Dev Biol |
Title: |
Differential requirements for neurogenin 3 in the development of POMC and NPY neurons in the hypothalamus. |
Volume: |
349 |
Issue: |
2 |
Pages: |
406-16 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kashimada K |
Year: |
2011 |
Journal: |
FASEB J |
Title: |
Antagonistic regulation of Cyp26b1 by transcription factors SOX9/SF1 and FOXL2 during gonadal development in mice. |
Volume: |
25 |
Issue: |
10 |
Pages: |
3561-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Berger A |
Year: |
2016 |
Journal: |
Endocrinology |
Title: |
Gsα Deficiency in the Ventromedial Hypothalamus Enhances Leptin Sensitivity and Improves Glucose Homeostasis in Mice on a High-Fat Diet. |
Volume: |
157 |
Issue: |
2 |
Pages: |
600-10 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yadav VK |
Year: |
2022 |
Journal: |
J Clin Invest |
Title: |
Embryonic osteocalcin signaling determines lifelong adrenal steroidogenesis and homeostasis in the mouse. |
Volume: |
132 |
Issue: |
4 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Fagan MP |
Year: |
2020 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Essential and sex-specific effects of mGluR5 in ventromedial hypothalamus regulating estrogen signaling and glucose balance. |
Volume: |
117 |
Issue: |
32 |
Pages: |
19566-19577 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhao L |
Year: |
2001 |
Journal: |
Development |
Title: |
Steroidogenic factor 1 (SF1) is essential for pituitary gonadotrope function. |
Volume: |
128 |
Issue: |
2 |
Pages: |
147-54 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ellsworth BS |
Year: |
2008 |
Journal: |
Dev Biol |
Title: |
Mechanisms underlying pituitary hypoplasia and failed cell specification in Lhx3-deficient mice. |
Volume: |
313 |
Issue: |
1 |
Pages: |
118-29 |
|
•
•
•
•
•
|
Publication |
First Author: |
Liu W |
Year: |
2023 |
Journal: |
Sci Rep |
Title: |
A novel monoclonal antibody against 6-sulfo sialyl Lewis x glycans attenuates murine allergic rhinitis by suppressing Th2 immune responses. |
Volume: |
13 |
Issue: |
1 |
Pages: |
15740 |
|
•
•
•
•
•
|
Publication |
First Author: |
Quenneville S |
Year: |
2020 |
Journal: |
Diabetes |
Title: |
Hypoglycemia-Sensing Neurons of the Ventromedial Hypothalamus Require AMPK-Induced Txn2 Expression but Are Dispensable for Physiological Counterregulation. |
Volume: |
69 |
Issue: |
11 |
Pages: |
2253-2266 |
|
•
•
•
•
•
|
Publication |
First Author: |
Brix LM |
Year: |
2022 |
Journal: |
Mol Metab |
Title: |
Contribution of the co-chaperone FKBP51 in the ventromedial hypothalamus to metabolic homeostasis in male and female mice. |
Volume: |
65 |
|
Pages: |
101579 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pulichino AM |
Year: |
2003 |
Journal: |
Genes Dev |
Title: |
Tpit determines alternate fates during pituitary cell differentiation. |
Volume: |
17 |
Issue: |
6 |
Pages: |
738-47 |
|
•
•
•
•
•
|
Publication |
First Author: |
Walczak EM |
Year: |
2014 |
Journal: |
Mol Endocrinol |
Title: |
Wnt signaling inhibits adrenal steroidogenesis by cell-autonomous and non-cell-autonomous mechanisms. |
Volume: |
28 |
Issue: |
9 |
Pages: |
1471-86 |
|
•
•
•
•
•
|
Publication |
First Author: |
Cheung CC |
Year: |
2013 |
Journal: |
J Comp Neurol |
Title: |
Genetic labeling of steroidogenic factor-1 (SF-1) neurons in mice reveals ventromedial nucleus of the hypothalamus (VMH) circuitry beginning at neurogenesis and development of a separate non-SF-1 neuronal cluster in the ventrolateral VMH. |
Volume: |
521 |
Issue: |
6 |
Pages: |
1268-88 |
|
•
•
•
•
•
|
Publication |
First Author: |
Furigo IC |
Year: |
2019 |
Journal: |
FASEB J |
Title: |
Growth hormone enhances the recovery of hypoglycemia via ventromedial hypothalamic neurons. |
Volume: |
33 |
Issue: |
11 |
Pages: |
11909-11924 |
|
•
•
•
•
•
|
Publication |
First Author: |
Steinbusch LK |
Year: |
2016 |
Journal: |
Diabetes |
Title: |
Sex-Specific Control of Fat Mass and Counterregulation by Hypothalamic Glucokinase. |
Volume: |
65 |
Issue: |
10 |
Pages: |
2920-31 |
|
•
•
•
•
•
|
Publication |
First Author: |
Felsted JA |
Year: |
2020 |
Journal: |
Endocrinology |
Title: |
Sex-specific Effects of α2δ-1 in the Ventromedial Hypothalamus of Female Mice Controlling Glucose and Lipid Balance. |
Volume: |
161 |
Issue: |
7 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Pedroso JAB |
Year: |
2021 |
Journal: |
Peptides |
Title: |
Deletion of growth hormone receptor in hypothalamic neurons affects the adaptation capacity to aerobic exercise. |
Volume: |
135 |
|
Pages: |
170426 |
|
•
•
•
•
•
|
Publication |
First Author: |
Du X |
Year: |
2002 |
Journal: |
Biochim Biophys Acta |
Title: |
The LIM-only coactivator FHL2 modulates WT1 transcriptional activity during gonadal differentiation. |
Volume: |
1577 |
Issue: |
1 |
Pages: |
93-101 |
|
•
•
•
•
•
|
Publication |
First Author: |
Whitworth DJ |
Year: |
2001 |
Journal: |
Gene |
Title: |
Characterization of steroidogenic factor 1 during sexual differentiation in a marsupial. |
Volume: |
277 |
Issue: |
1-2 |
Pages: |
209-19 |
|
•
•
•
•
•
|
Publication |
First Author: |
Western PS |
Year: |
2000 |
Journal: |
Gene |
Title: |
Temperature-dependent sex determination in the American alligator: expression of SF1, WT1 and DAX1 during gonadogenesis. |
Volume: |
241 |
Issue: |
2 |
Pages: |
223-32 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lahbib-Mansais Y |
Year: |
1997 |
Journal: |
Cytogenet Cell Genet |
Title: |
Mapping in pig of genes involved in sexual differentiation: AMH, WT1, FTZF1, SOX2, SOX9, AHC, and placental and embryonic CYP19. |
Volume: |
76 |
Issue: |
1-2 |
Pages: |
109-14 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wood WM |
Year: |
1998 |
Journal: |
Mol Cell Endocrinol |
Title: |
Functional interactions of an upstream enhancer of the mouse glycoprotein hormone alpha-subunit gene with proximal promoter sequences. |
Volume: |
142 |
Issue: |
1-2 |
Pages: |
141-52 |
|
•
•
•
•
•
|
Publication |
First Author: |
Toyooka Y |
Year: |
1998 |
Journal: |
Int J Dev Biol |
Title: |
Wilms' tumor suppressor gene (WT1) as a target gene of SRY function in a mouse ES cell line transfected with SRY. |
Volume: |
42 |
Issue: |
8 |
Pages: |
1143-51 |
|
•
•
•
•
•
|
Publication |
First Author: |
Pieri I |
Year: |
1999 |
Journal: |
Eur J Neurosci |
Title: |
Regulation of the murine NMDA-receptor-subunit NR2C promoter by Sp1 and fushi tarazu factor1 (FTZ-F1) homologues. |
Volume: |
11 |
Issue: |
6 |
Pages: |
2083-92 |
|
•
•
•
•
•
|
Publication |
First Author: |
Jin Z |
Year: |
2009 |
Journal: |
J Biol Chem |
Title: |
Different transcription factors regulate nestin gene expression during P19 cell neural differentiation and central nervous system development. |
Volume: |
284 |
Issue: |
12 |
Pages: |
8160-73 |
|
•
•
•
•
•
|
Publication |
First Author: |
Gao L |
Year: |
2011 |
Journal: |
Biol Reprod |
Title: |
Two regions within the proximal steroidogenic factor 1 promoter drive somatic cell-specific activity in developing gonads of the female mouse. |
Volume: |
84 |
Issue: |
3 |
Pages: |
422-34 |
|
•
•
•
•
•
|
Publication |
First Author: |
Munger SC |
Year: |
2013 |
Journal: |
PLoS Genet |
Title: |
Fine time course expression analysis identifies cascades of activation and repression and maps a putative regulator of mammalian sex determination. |
Volume: |
9 |
Issue: |
7 |
Pages: |
e1003630 |
|
•
•
•
•
•
|
Publication |
First Author: |
Choi H |
Year: |
2019 |
Journal: |
Am J Physiol Endocrinol Metab |
Title: |
Krüppel-like factor 4 plays a role in the luteal transition in steroidogenesis by downregulating Cyp19A1 expression. |
Volume: |
316 |
Issue: |
6 |
Pages: |
E1071-E1080 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
104
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Toone WM |
Year: |
1991 |
Journal: |
J Bacteriol |
Title: |
deaD, a new Escherichia coli gene encoding a presumed ATP-dependent RNA helicase, can suppress a mutation in rpsB, the gene encoding ribosomal protein S2. |
Volume: |
173 |
Issue: |
11 |
Pages: |
3291-302 |
|
•
•
•
•
•
|
Publication |
First Author: |
Charollais J |
Year: |
2004 |
Journal: |
Nucleic Acids Res |
Title: |
CsdA, a cold-shock RNA helicase from Escherichia coli, is involved in the biogenesis of 50S ribosomal subunit. |
Volume: |
32 |
Issue: |
9 |
Pages: |
2751-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Jain C |
Year: |
2008 |
Journal: |
RNA |
Title: |
The E. coli RhlE RNA helicase regulates the function of related RNA helicases during ribosome assembly. |
Volume: |
14 |
Issue: |
2 |
Pages: |
381-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhang Y |
Year: |
2013 |
Journal: |
Nucleic Acids Res |
Title: |
Structure, phosphorylation and U2AF65 binding of the N-terminal domain of splicing factor 1 during 3'-splice site recognition. |
Volume: |
41 |
Issue: |
2 |
Pages: |
1343-54 |
|
•
•
•
•
•
|
Publication |
First Author: |
Corsini L |
Year: |
2007 |
Journal: |
Nat Struct Mol Biol |
Title: |
U2AF-homology motif interactions are required for alternative splicing regulation by SPF45. |
Volume: |
14 |
Issue: |
7 |
Pages: |
620-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Horikoshi N |
Year: |
2010 |
Journal: |
Genes Cells |
Title: |
Holliday junction-binding activity of human SPF45. |
Volume: |
15 |
Issue: |
4 |
Pages: |
373-83 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chaouki AS |
Year: |
2006 |
Journal: |
PLoS Genet |
Title: |
Drosophila SPF45: a bifunctional protein with roles in both splicing and DNA repair. |
Volume: |
2 |
Issue: |
12 |
Pages: |
e178 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
This entry represents a group of helicases, including DNA2 and Nam7. Proteins in this family contain a conserved domain with s a P-loop motif that is characteristic of the AAA superfamily. They are DEAD-like helicases belonging to superfamily (SF)1, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. Similar to SF2 helicases, SF1 helicases do not form toroidal structures like SF3-6 helicases. Their helicase core consists of two similar protein domains that resemble the fold of the recombination protein RecA [, , ].Dna2 is a DNA replication factor with single-stranded DNA-dependent ATPase, ATP-dependent nuclease, (5'-flap endonuclease) and helicase activities [, ]. Nam7 (also known as Upf1) is an ATP-dependent RNA helicase involved in the nonsense-mediated mRNA decay (NMD) pathway []. |
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•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
RNA helicases from the DEAD-box family are found in almost all organisms andhave important roles in RNA metabolism, such as splicing, RNA transport,ribosome biogenesis, translation and RNA decay. They are enzymes that unwinddouble-stranded RNA molecules in an energy dependent fashion through thehydrolysis of NTP. DEAD-box RNA helicases belong to superfamily 2 (SF2) ofhelicases. As other SF1 and SF2 members they contain seven conserved motifswhich are characteristic of these two superfamilies [].DEAD-box is named after the amino acids of motif II or Walker B (Mg2+-bindingaspartic acid). The RNA helicase DeaD is ATP-dependent []and is induced by low temperatures []. In addition to its role in unwinding double stranded RNA, it is involved in ribosomal subunit biogenesis []. |
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•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
RNA helicases from the DEAD-box family are found in almost all organisms andhave important roles in RNA metabolism, such as splicing, RNA transport,ribosome biogenesis, translation and RNA decay. They are enzymes that unwinddouble-stranded RNA molecules in an energy dependent fashion through thehydrolysis of NTP. DEAD-box RNA helicases belong to superfamily 2 (SF2) ofhelicases. As other SF1 and SF2 members they contain seven conserved motifswhich are characteristic of these two superfamilies [].DEAD-box is named after the amino acids of motif II or Walker B (Mg2+-bindingaspartic acid). RhlE is a DEAD-box RNA helicase that is involved in ribosome assembly. It may play a role in the interconversion of ribosomal RNA-folding intermediates that are further processed by DeaD or SrmB during ribosome maturation []. |
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•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
This domain contains a P-loop motif that is characteristic of the AAA superfamily. Proteins containing this domain are DEAD-like helicases belonging to superfamily (SF)1, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. Similar to SF2 helicases, SF1 helicases do not form toroidal structures like SF3-6 helicases. Their helicase core consists of two similar protein domains that resemble the fold of the recombination protein RecA [, , ].Proteins containing this domain include helicases, such as Dna2 an Nam7. Dna2 is a DNA replication factor with single-stranded DNA-dependent ATPase, ATP-dependent nuclease, (5'-flap endonuclease) and helicase activities [, ]. Nam7 (also known as Upf1) is an ATP-dependent RNA helicase involved in the nonsense-mediated mRNA decay (NMD) pathway []. This domain can also be found in some virus polyproteins. This domain is also known as HelicC. |
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•
•
•
•
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Protein Domain |
Type: |
Domain |
Description: |
This entry represents the RNA recognition motif (RRM) of SPF45. SPF45, also termed RNA-binding motif protein 17 (RBM17), is an RNA-binding protein consisting of an unstructured N-terminal region, followed by a G-patch motif and a C-terminal U2AF (U2 auxiliary factor) homology motifs (UHM) that harbours a RNA recognition motif (RRM) and an Arg-Xaa-Phe sequence motif. SPF45 is a bifunctional protein that functions in splicing and DNA repair. It is involved in regulating alternative splicing of the apoptosis regulatory gene FAS (also called CD95). Its UHM binds UHM-ligand motifs (ULMs) present in the 3' splice site-recognizing factors U2AF65, SF1 and SF3b155 []. It binds to the Holliday junction, which is a key DNA intermediate in the homologous-recombination pathway [, ]. |
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•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
Nidoviruses (Coronaviridae, Arteriviridae, and Roniviridae) feature the most complex genetic organization among plus-strand RNA viruses. Their replicase genes encode an exceptionally large replicase polyprotein 1a/ab which is then proteolytically processed to release different nonstructural proteins (NSPs) that mediate the key functions required for replication and transcription. One of these NSPs, called NSP10 in arteriviruses (Av) and NSP13 in coronaviruses (CoV) functions as a helicase [, ]. It is a multidomain protein consisting of a N-terminal Cys/His rich zinc-binding domain (ZBD) and a helicase core that belongs to the superfamily SF1 of helicases. The helicase core contains two RecA1 and RecA2 domains and a 1B domain [].This entry represents the 1B domain, which has a regulatory role modulating the nucleic acid substrate binding. Based on the structures from the Equine arteritis virus (EAV) NSP10, 1B domain undergoes large conformational change upon substrate binding, and forms a channel together with 1A and 2A domains that accommodates the single stranded nucleic acids [, ]. |
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•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
This helix-hairpin domain can be found in N-terminal region of mammalian splicing factor 1 (SF1) and fungal branchpoint binding proteins (BBP) []. These proteins are required for pre-spliceosome formation, which is the first step of pre-mRNA splicing [, ]. SF1 forms a complex with U2AF65 through the interaction between this domain and the C-terminal U2AF homology motif domain (UHM) of U2AF65. This domain forms a secondary, hydrophobic interface with U2AF65(UHM) to lock the orientation of the two subunits, which is essential for cooperative formation of the ternary SF1-U2AF65-RNA complex []. This domain contains a highly conserved SPSP motif at its C terminus; the phophorylation of the SPSP motif induces a disorder-to-order transition within a novel SF1/U2AF65 interface []. |
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•
•
•
•
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Protein Domain |
Type: |
Domain |
Description: |
Helicases have been classified in 5 superfamilies (SF1-SF5). For the two largest groups, commonly referred to as SF1 and SF2, a total of seven characteristic motifs has been identified []. These two superfamilies encompass a large number of DNA and RNA helicases from archaea, eubacteria, eukaryotes and viruses.This entry represents the C-terminal domain found in proteins belonging to the helicase superfamilies 1 and 2. Included in this group is the eukaryotic translation initiation factor 4A (eIF4A), a member of the DEA(D/H)-box RNA helicase family. The structure of the carboxyl-terminal domain of eIF4A has been determined; it has a parallel α-β topology that superimposes, with minor variations, on the structures and conserved motifs of the equivalent domain in other, distantly related helicases []. |
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•
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•
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Publication |
First Author: |
Fuller-Pace FV |
Year: |
2006 |
Journal: |
Nucleic Acids Res |
Title: |
DExD/H box RNA helicases: multifunctional proteins with important roles in transcriptional regulation. |
Volume: |
34 |
Issue: |
15 |
Pages: |
4206-15 |
|
•
•
•
•
•
|
Publication |
First Author: |
de la Cruz J |
Year: |
1999 |
Journal: |
Trends Biochem Sci |
Title: |
Unwinding RNA in Saccharomyces cerevisiae: DEAD-box proteins and related families. |
Volume: |
24 |
Issue: |
5 |
Pages: |
192-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Koonin EV |
Year: |
1992 |
Journal: |
FEBS Lett |
Title: |
Autogenous translation regulation by Escherichia coli ATPase SecA may be mediated by an intrinsic RNA helicase activity of this protein. |
Volume: |
298 |
Issue: |
1 |
Pages: |
6-8 |
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•
•
•
•
•
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Publication |
First Author: |
Correa SM |
Year: |
2012 |
Journal: |
PLoS Genet |
Title: |
Sex reversal in C57BL/6J XY mice caused by increased expression of ovarian genes and insufficient activation of the testis determining pathway. |
Volume: |
8 |
Issue: |
4 |
Pages: |
e1002569 |
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•
•
•
•
•
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Publication |
First Author: |
Büdefeld T |
Year: |
2011 |
Journal: |
Exp Neurol |
Title: |
Altered position of cell bodies and fibers in the ventromedial region in SF-1 knockout mice. |
Volume: |
232 |
Issue: |
2 |
Pages: |
176-84 |
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•
•
•
•
•
|
Publication |
First Author: |
Achermann JC |
Year: |
2001 |
Journal: |
Mol Cell Endocrinol |
Title: |
Phenotypic spectrum of mutations in DAX-1 and SF-1. |
Volume: |
185 |
Issue: |
1-2 |
Pages: |
17-25 |
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•
•
•
•
•
|
Publication |
First Author: |
Baldo B |
Year: |
2014 |
Journal: |
PLoS One |
Title: |
Effects of deletion of mutant huntingtin in steroidogenic factor 1 neurons on the psychiatric and metabolic phenotype in the BACHD mouse model of Huntington disease. |
Volume: |
9 |
Issue: |
10 |
Pages: |
e107691 |
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•
•
•
•
•
|
Publication |
First Author: |
Agrimson KS |
Year: |
2022 |
Journal: |
PLoS Genet |
Title: |
Lrh1 can help reprogram sexual cell fate and is required for Sertoli cell development and spermatogenesis in the mouse testis. |
Volume: |
18 |
Issue: |
2 |
Pages: |
e1010088 |
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•
•
•
•
•
|
Publication |
First Author: |
Meng A |
Year: |
2023 |
Journal: |
J Neurosci |
Title: |
mGluR5 in Astrocytes in the Ventromedial Hypothalamus Regulates Pituitary Adenylate Cyclase-Activating Polypeptide Neurons and Glucose Homeostasis. |
Volume: |
43 |
Issue: |
33 |
Pages: |
5918-5935 |
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•
•
•
•
•
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Publication |
First Author: |
Cammas FM |
Year: |
1997 |
Journal: |
Mol Endocrinol |
Title: |
The mouse adrenocorticotropin receptor gene: cloning and characterization of its promoter and evidence for a role for the orphan nuclear receptor steroidogenic factor 1. |
Volume: |
11 |
Issue: |
7 |
Pages: |
867-76 |
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•
•
•
•
•
|
Publication |
First Author: |
Caruthers JM |
Year: |
2000 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Crystal structure of yeast initiation factor 4A, a DEAD-box RNA helicase. |
Volume: |
97 |
Issue: |
24 |
Pages: |
13080-5 |
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•
•
•
•
•
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Publication |
First Author: |
Caruthers JM |
Year: |
2002 |
Journal: |
Curr Opin Struct Biol |
Title: |
Helicase structure and mechanism. |
Volume: |
12 |
Issue: |
1 |
Pages: |
123-33 |
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•
•
•
•
•
|
Publication |
First Author: |
Tanner NK |
Year: |
2001 |
Journal: |
Mol Cell |
Title: |
DExD/H box RNA helicases: from generic motors to specific dissociation functions. |
Volume: |
8 |
Issue: |
2 |
Pages: |
251-62 |
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•
•
•
•
•
|
Publication |
First Author: |
Koonin EV |
Year: |
1993 |
Journal: |
Nucleic Acids Res |
Title: |
Escherichia coli dinG gene encodes a putative DNA helicase related to a group of eukaryotic helicases including Rad3 protein. |
Volume: |
21 |
Issue: |
6 |
Pages: |
1497 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
34
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Gorbalenya AE |
Year: |
1989 |
Journal: |
Nucleic Acids Res |
Title: |
Two related superfamilies of putative helicases involved in replication, recombination, repair and expression of DNA and RNA genomes. |
Volume: |
17 |
Issue: |
12 |
Pages: |
4713-30 |
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•
•
•
•
•
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Protein Domain |
Type: |
Domain |
Description: |
Helicases have been classified in 5 superfamilies (SF1-SF5). All of the proteins bind ATP and, consequently, all of them carry the classical Walker A(phosphate-binding loop or P-loop) and Walker B(Mg2+-binding aspartic acid) motifs. For the two largest groups, commonlyreferred to as SF1 and SF2, a total of seven characteristic motifs has beenidentified []. These two superfamilies encompass a large number of DNA andRNA helicases from archaea, eubacteria, eukaryotes and viruses that seem to beactive as monomers or dimers. RNA and DNA helicases are considered to beenzymes that catalyze the separation of double-stranded nucleic acids in anenergy-dependent manner [].The various structures of SF1 and SF2 helicases present a common core with twoα-β RecA-like domains [, ]. Thestructural homology with the RecA recombination protein covers the fivecontiguous parallel beta strands and the tandem alpha helices. ATP binds tothe amino proximal α-β domain, where the Walker A (motif I) and WalkerB (motif II) are found. The N-terminal domain also contains motif III (S-A-T)which was proposed to participate in linking ATPase and helicase activities.The carboxy-terminal α-β domain is structurally very similar to theproximal one even though it is bereft of an ATP-binding site, suggesting thatit may have originally arisen through gene duplication of the first one.Some members of helicase superfamilies 1 and 2 are listed below:DEAD-box RNA helicases. The prototype of DEAD-boxproteins is the translation initiation factor eIF4A. The eIF4A protein isan RNA-dependent ATPase which functions together with eIF4B as an RNAhelicase [].DEAH-box RNA helicases. Mainly pre-mRNA-splicing factorATP-dependent RNA helicases [].Eukaryotic DNA repair helicase RAD3/ERCC-2, an ATP-dependent 5'-3' DNAhelicase involved in nucleotide excision repair of UV-damaged DNA.Eukaryotic TFIIH basal transcription factor complex helicase XPB subunit.An ATP-dependent 3'-5' DNA helicase which is a component of the core-TFIIHbasal transcription factor, involved in nucleotide excision repair (NER) ofDNA and, when complexed to CAK, in RNA transcription by RNA polymerase II.It acts by opening DNA either around the RNA transcription start site orthe DNA.Eukaryotic ATP-dependent DNA helicase Q. A DNA helicase that may play arole in the repair of DNA that is damaged by ultraviolet light or othermutagens.Bacterial and eukaryotic antiviral SKI2-like helicase. SKI2 has a role inthe 3'-mRNA degradation pathway, repressing dsRNA virus propagation byspecifically blocking translation of viral mRNAs, perhaps recognizing theabsence of CAP or poly(A).Bacterial DNA-damage-inducible protein G (DinG). A probable helicaseinvolved in DNA repair and perhaps also replication [].Bacterial primosomal protein N' (PriA). PriA protein is one of sevenproteins that make up the restart primosome, an apparatus that promotesassembly of replisomes at recombination intermediates and stalledreplication forks.Bacterial ATP-dependent DNA helicase recG. It has a critical role inrecombination and DNA repair, helping process Holliday junctionintermediates to mature products by catalyzing branch migration. It has aDNA unwinding activity characteristic of helicases with a 3' to 5'polarity.A variety of DNA and RNA virus helicases and transcription factorsThis entry represents the DNA-binding domain of classical SF1 and SF2 helicases. It does not recognize bacterial DinG and eukaryotic Rad3 which differ from other SF1-SF2 helicases by the presence of a large insert after the Walker A (see ). |
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•
•
•
•
•
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Protein Domain |
Type: |
Domain |
Description: |
Helicases have been classified in 5 superfamilies (SF1-SF5). All of the proteins bind ATP and, consequently, all of them carry the classical Walker A(phosphate-binding loop or P-loop) and Walker B(Mg2+-binding aspartic acid) motifs. For the two largest groups, commonlyreferred to as SF1 and SF2, a total of seven characteristic motifs has beenidentified []. These two superfamilies encompass a large number of DNA andRNA helicases from archaea, eubacteria, eukaryotes and viruses that seem to beactive as monomers or dimers. RNA and DNA helicases are considered to beenzymes that catalyze the separation of double-stranded nucleic acids in anenergy-dependent manner [].The various structures of SF1 and SF2 helicases present a common core with twoα-β RecA-like domains [, ]. Thestructural homology with the RecA recombination protein covers the fivecontiguous parallel beta strands and the tandem alpha helices. ATP binds tothe amino proximal α-β domain, where the Walker A (motif I) and WalkerB (motif II) are found. The N-terminal domain also contains motif III (S-A-T)which was proposed to participate in linking ATPase and helicase activities.The carboxy-terminal α-β domain is structurally very similar to theproximal one even though it is bereft of an ATP-binding site, suggesting thatit may have originally arisen through gene duplication of the first one.Some members of helicase superfamilies 1 and 2 are listed below:DEAD-box RNA helicases. The prototype ofDEAD-boxproteins is the translation initiation factor eIF4A. The eIF4A protein isan RNA-dependent ATPase which functions together with eIF4B as an RNAhelicase [].DEAH-box RNA helicases. Mainly pre-mRNA-splicing factorATP-dependent RNA helicases [].Eukaryotic DNA repair helicase RAD3/ERCC-2, an ATP-dependent 5'-3' DNAhelicase involved in nucleotide excision repair of UV-damaged DNA.Eukaryotic TFIIH basal transcription factor complex helicase XPB subunit.An ATP-dependent 3'-5' DNA helicase which is a component of the core-TFIIHbasal transcription factor, involved in nucleotide excision repair (NER) ofDNA and, when complexed to CAK, in RNA transcription by RNA polymerase II.It acts by opening DNA either around the RNA transcription start site orthe DNA.Eukaryotic ATP-dependent DNA helicase Q. A DNA helicase that may play arole in the repair of DNA that is damaged by ultraviolet light or othermutagens.Bacterial and eukaryotic antiviral SKI2-like helicase. SKI2 has a role inthe 3'-mRNA degradation pathway, repressing dsRNA virus propagation byspecifically blocking translation of viral mRNAs, perhaps recognizing theabsence of CAP or poly(A).Bacterial DNA-damage-inducible protein G (DinG). A probable helicaseinvolved in DNA repair and perhaps also replication [].Bacterial primosomal protein N' (PriA). PriA protein is one of sevenproteins that make up the restart primosome, an apparatus that promotesassembly of replisomes at recombination intermediates and stalledreplication forks.Bacterial ATP-dependent DNA helicase recG. It has a critical role inrecombination and DNA repair, helping process Holliday junctionintermediates to mature products by catalyzing branch migration. It has aDNA unwinding activity characteristic of helicases with a 3' to 5'polarity.A variety of DNA and RNA virus helicases and transcription factorsThis entry represents the ATP-binding domain found within bacterial DinG and eukaryotic Rad3 proteins, differing from other SF1 and SF2 helicases by the presence of a large insert after the Walker A motif []. |
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•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Helicases have been classified in 5 superfamilies (SF1-SF5). All of the proteins bind ATP and, consequently, all of them carry the classical Walker A(phosphate-binding loop or P-loop) and Walker B(Mg2+-binding aspartic acid) motifs. For the two largest groups, commonlyreferred to as SF1 and SF2, a total of seven characteristic motifs has beenidentified []. These two superfamilies encompass a large number of DNA andRNA helicases from archaea, eubacteria, eukaryotes and viruses that seem to beactive as monomers or dimers. RNA and DNA helicases are considered to beenzymes that catalyze the separation of double-stranded nucleic acids in anenergy-dependent manner [].The various structures of SF1 and SF2 helicases present a common core with twoα-β RecA-like domains [, ]. Thestructural homology with the RecA recombination protein covers the fivecontiguous parallel beta strands and the tandem alpha helices. ATP binds tothe amino proximal α-β domain, where the Walker A (motif I) and WalkerB (motif II) are found. The N-terminal domain also contains motif III (S-A-T)which was proposed to participate in linking ATPase and helicase activities.The carboxy-terminal α-β domain is structurally very similar to theproximal one even though it is bereft of an ATP-binding site, suggesting thatit may have originally arisen through gene duplication of the first one.Some members of helicase superfamilies 1 and 2 are listed below:DEAD-box RNA helicases. The prototype of DEAD-boxproteins is the translation initiation factor eIF4A. The eIF4A protein isan RNA-dependent ATPase which functions together with eIF4B as an RNAhelicase [].DEAH-box RNA helicases. Mainly pre-mRNA-splicing factorATP-dependent RNA helicases [].Eukaryotic DNA repair helicase RAD3/ERCC-2, an ATP-dependent 5'-3' DNAhelicase involved in nucleotide excision repair of UV-damaged DNA.Eukaryotic TFIIH basal transcription factor complex helicase XPB subunit.An ATP-dependent 3'-5' DNA helicase which is a component of the core-TFIIHbasal transcription factor, involved in nucleotide excision repair (NER) ofDNA and, when complexed to CAK, in RNA transcription by RNA polymerase II.It acts by opening DNA either around the RNA transcription start site orthe DNA.Eukaryotic ATP-dependent DNA helicase Q. A DNA helicase that may play arole in the repair of DNA that is damaged by ultraviolet light or othermutagens.Bacterial and eukaryotic antiviral SKI2-like helicase. SKI2 has a role inthe 3'-mRNA degradation pathway, repressing dsRNA virus propagation byspecifically blocking translation of viral mRNAs, perhaps recognizing theabsence of CAP or poly(A).Bacterial DNA-damage-inducible protein G (DinG). A probable helicaseinvolved in DNA repair and perhaps also replication [].Bacterial primosomal protein N' (PriA). PriA protein is one of sevenproteins that make up the restart primosome, an apparatus that promotesassembly of replisomes at recombination intermediates and stalledreplication forks.Bacterial ATP-dependent DNA helicase recG. It has a critical role inrecombination and DNA repair, helping process Holliday junctionintermediates to mature products by catalyzing branch migration. It has aDNA unwinding activity characteristic of helicases with a 3' to 5'polarity.A variety of DNA and RNA virus helicases and transcription factorsThis entry includes bacterial DinG and eukaryotic Rad3 proteins, differing from other SF1 and SF2 helicases by the presence of a large insert after the Walker A motif []. |
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•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
87
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
237
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
M Plank TD |
Year: |
2018 |
Journal: |
Bioessays |
Title: |
RNA Decay Factor UPF1 Promotes Protein Decay: A Hidden Talent. |
Volume: |
40 |
Issue: |
1 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Zhou D |
Year: |
2005 |
Journal: |
Gene |
Title: |
Transcriptional regulation of the mouse PNRC2 promoter by the nuclear factor Y (NFY) and E2F1. |
Volume: |
361 |
|
Pages: |
89-100 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
639
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
886
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
747
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1145
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1069
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1240
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1481
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1040
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1145
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
286
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
972
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
505
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1710
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1145
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
229
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
616
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
323
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
540
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
312
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
482
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1711
 |
Fragment?: |
false |
|
•
•
•
•
•
|