A novel docking site on Mediator is critical for activation by VP16 in mammalian cells - Wikidata - wikimedia - TriplyDB

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

http://www.wikidata.org/entity/Q24594322

about

Mediator modulates Gli3-dependent Sonic hedgehog signaling MED25 is distinct from TRAP220/MED1 in cooperating with CBP for retinoid receptor activation PTOV1 enables the nuclear translocation and mitogenic activity of flotillin-1, a major protein of lipid rafts MED19 and MED26 are synergistic functional targets of the RE1 silencing transcription factor in epigenetic silencing of neuronal gene expression Interaction of Bunyamwera Orthobunyavirus NSs protein with mediator protein MED8: a mechanism for inhibiting the interferon response Mediator-dependent nuclear receptor function The potential link between PML NBs and ICP0 in regulating lytic and latent infection of HSV-1 Structure and VP16 binding of the Mediator Med25 activator interaction domain Structure of the VP16 transactivator target in the Mediator Solution NMR structure of MED25(391–543) comprising the activator-interacting domain (ACID) of human mediator subunit 25 The Acidic Transcription Activator Gcn4 Binds the Mediator Subunit Gal11/Med15 Using a Simple Protein Interface Forming a Fuzzy Complex Mechanism of Mediator recruitment by tandem Gcn4 activation domains and three Gal11 activator-binding domains The Mediator complex and transcription regulation The mammalian Mediator complex Interaction studies of the human and Arabidopsis thaliana Med25-ACID proteins with the herpes simplex virus VP16- and plant-specific Dreb2a transcription factors Characterization of ERM transactivation domain binding to the ACID/PTOV domain of the Mediator subunit MED25 Complexity in transcription control at the activation domain-mediator interface.A sequence-specific transcription activator motif and powerful synthetic variants that bind Mediator using a fuzzy protein interface.Two modes of transcriptional activation at native promoters by NF-kappaB p65 Herpes simplex virus VP16, but not ICP0, is required to reduce histone occupancy and enhance histone acetylation on viral genomes in U2OS osteosarcoma cells.Inhibition of SREBP transcriptional activity by a boron-containing compound improves lipid homeostasis in diet-induced obesity Mediator and human disease Genome-Scale CRISPR-Mediated Control of Gene Repression and Activation Med25 is required for RNA polymerase II recruitment to specific promoters, thus regulating xenobiotic and lipid metabolism in human liver.Function and regulation of the Mediator complex.A systematic analysis of host factors reveals a Med23-interferon-λ regulatory axis against herpes simplex virus type 1 replication.The Arabidopsis thaliana Med25 mediator subunit integrates environmental cues to control plant development.Promoter activation by the varicella-zoster virus major transactivator IE62 and the cellular transcription factor USF.Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors.Phosphorylation of the VP16 transcriptional activator protein during herpes simplex virus infection and mutational analysis of putative phosphorylation sites.Identification of a common epitope between enterovirus 71 and human MED25 proteins which may explain virus-associated neurological disease.Proteomic analysis of the herpes simplex virus 1 virion protein 16 transactivator protein in infected cells Barrier-to-Autointegration Factor 1 (BAF/BANF1) Promotes Association of the SETD1A Histone Methyltransferase with Herpes Simplex Virus Immediate-Early Gene Promoters.Reactivation of MASPIN in non-small cell lung carcinoma (NSCLC) cells by artificial transcription factors (ATFs)Mediator subunits MED1 and MED24 cooperatively contribute to pubertal mammary gland development and growth of breast carcinoma cells.An activation domain within the walleye dermal sarcoma virus retroviral cyclin protein is essential for inhibition of the viral promoter.Endoplasmic reticulum stress-responsive transcription factor ATF6α directs recruitment of the Mediator of RNA polymerase II transcription and multiple histone acetyltransferase complexes.Comparative genomics supports a deep evolutionary origin for the large, four-module transcriptional mediator complex Varicella-zoster virus IE62 protein utilizes the human mediator complex in promoter activation.The dynamics of HCF-1 modulation of herpes simplex virus chromatin during initiation of infection.

P2860

Q24304401-81F802F3-294C-4E91-8F30-C179DECF50A4 Q24321381-61CF6C16-86FA-41D3-AB76-F1D78B52F2C6 Q24556632-4FE7C2BF-44D0-487C-A429-17E49CF2E6D4 Q24644562-23BA47E4-0294-4646-B82E-8F5B215A17E6 Q24670740-9A5C98E0-19E8-4D21-9FD5-727669EA7B2E Q26995848-8FFF0282-5483-4E28-888D-B218F7D73435 Q27027918-1AD963DC-3C7D-43DF-B41C-B40912F8CC0B Q27666881-FB65E035-04B1-48D9-B87D-496CD4BFDFDB Q27667187-1CF5FB24-88B8-4774-A193-28A54A1F8DE3 Q27670982-F0EA70C5-3AE5-40DD-A0F4-AF568CF5442D Q27676397-CDEA7929-1A53-410A-A189-3E8523593E07 Q27932233-1A177206-E0F8-408F-872D-B7F139BF6CA6 Q28299679-AB15A928-9AFE-478B-8F48-9980CC9B7A80 Q28304955-9DD146B3-E4AD-4B86-9895-A693FD9FC00C Q28539189-19C5ED9E-004C-4802-98FE-0A0A394E0A6C Q28610740-C6E125C1-9390-464E-A782-D068310F8DDF Q30491504-BD494F78-1AF5-4092-AE0A-18E02F8412F3 Q30586807-818B0BDE-C77E-42D7-8D07-063D442E9BF8 Q33425417-389BED31-179D-4A5C-9D38-E34247EF0213 Q33614347-FEB694D7-39BA-4D2C-AC0C-155BE72138AC Q33789340-9600383C-C05F-48FC-A767-8D2EB30F2188 Q33909044-654E9F2A-25DD-4524-8F6A-0989EC33F0D8 Q34443093-4CCA9D13-0A7A-4498-804C-625B53C0375C Q34528349-C6B523C2-B9D0-4A42-B7AD-91783005BAE6 Q34904976-3673C834-57EC-47FD-8E20-E8D61A1CF8FA Q34945388-B126FC97-D63F-428A-A675-F62268639C76 Q35002822-10DAAB17-E448-46B1-8FA1-E5E360B8193C Q35023792-7C0F7202-8B18-427A-BA04-A6FF4B526A08 Q35182494-54FAD960-B965-4D65-84DD-BD969C202D9B Q35253876-AA6A33EC-7308-4A5F-B289-36F9A065B31E Q35544351-9E8FCDD4-1CBD-4B42-A189-D03502163856 Q35586902-DD715207-EAFA-41E5-A5F3-27E91B125117 Q35660192-41CC9A86-45B5-404A-8A10-B4C9F3FBCD89 Q35754831-633D39DA-672C-4B1F-8E05-F47BE7A13A4C Q35867938-6BADD4D3-AEC2-4780-8E5D-0B58A0449A4D Q35998788-07247091-4EF4-4531-94E1-11F6E84FE83A Q36080483-D85BF2C5-D435-4031-8F07-9CF80A0D0FD0 Q36777813-67DD955A-2174-40AF-96DC-9D4E79C5EE7D Q36994683-1050A055-1752-4F02-85BA-D517202C1B8F Q37015734-7050FDC2-8874-4FAA-BA9B-B7FD4FBD7A06

P2860

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

http://www.wikidata.org/entity/Q24594322

description

2003 nî lūn-bûn

@nan

2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@ast

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@en

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@nl

type

label

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@ast

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@en

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@nl

prefLabel

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@ast

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@en

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@nl

P1433

Q24594322-D8F5E41A-0A6C-4FDF-A50E-95499FFE9ECF

P1476

Q24594322-1672F3C7-417C-40B6-9090-0D92000E8CB6

P2093

Q24594322-044AE3C6-41EE-4805-BFB9-FF723E2F9900

Q24594322-3A3F2509-CC8A-4E3B-BDBC-E70B37F40FAF

Q24594322-418E7CD6-23A2-45BA-8C4C-57143CA03548

Q24594322-58C24782-157C-49BF-9381-50E80CAD34DB

Q24594322-93EA95E4-B26B-4D1F-BE54-1F236A94EB8F

Q24594322-D4396CC0-1B18-4935-B36B-C8C859E3993F

Q24594322-E37C68D2-925F-4501-AB18-7AB4EAE4DF1F

P2860

Q24594322-0FB6995A-9BE9-4BF2-AFDF-E7A1E20B3ED9

Q24594322-13E1FC21-2955-4B4B-B68A-853664CB3C76

Q24594322-190D416E-7FC7-42DF-A82A-8395D83FE683

Q24594322-19F7A898-CE06-420A-B4F0-E24CFA0312F6

Q24594322-1D9B953A-4B60-40D7-99FE-5DCF739FA97F

Q24594322-2127E5F3-200B-4499-B8DF-63AA78C7C3C2

Q24594322-2374B5AB-5285-4BB7-B04A-1D82AFB0FC53

Q24594322-244F732E-75EB-4578-9783-335C4EA3EAAA

Q24594322-24B7C38D-3E98-4C26-9207-F8EBEFA62180

Q24594322-2C1253B0-7E03-4D96-AED6-EA32F1A09217

P304

Q24594322-8B1D6B6B-4DE4-4B7D-8929-BE2D6F22FFC6

P31

Q24594322-387B8643-98DE-4715-9DB1-8F8FAD4A4D58

P3181

Q24594322-08E9F48E-F44B-4E44-9CAE-48E52D5ED72F

P356

Q24594322-59F92E1A-2D12-40A8-9734-15D8052EF399

P407

Q24594322-0920BAD6-5CE8-47B3-B92F-A3B48D16F67E

P433

Q24594322-25FF2409-B53C-48A9-9BFA-C8A27AC29A65

P478

Q24594322-AAB9373D-922A-403D-9443-AD590B8AE16D

P50

Q24594322-DE00BCF5-CEC8-49C9-9F86-3C08DAB70AC6

P577

Q24594322-E1A2C94E-4E6E-4C8F-86DF-21B4DB31A8DC

P5875

Q24594322-4C29C9D0-AAFC-4D45-805A-C6DB836CA5DE

P698

Q24594322-82118D52-6AEF-45C5-A133-CF3E55B72B6E

P932

Q24594322-C41B4A3A-22B4-4D5B-8071-1786DDAF5581

P3181

P356

P1433

The EMBO Journal

P1476

A novel docking site on Mediator is critical for activation by VP16 in mammalian cells

@en

P2093

F Lottspeich

http://www.w3.org/2001/XMLSchema#string

Gerhard Mittler

http://www.w3.org/2001/XMLSchema#string

Lisa Santolin

http://www.w3.org/2001/XMLSchema#string

Lucia Berti

http://www.w3.org/2001/XMLSchema#string

Michael Meisterernst

http://www.w3.org/2001/XMLSchema#string

Thomas Stühler

http://www.w3.org/2001/XMLSchema#string

Thomas Uhlmann

http://www.w3.org/2001/XMLSchema#string

P2860

Identity between TRAP and SMCC complexes indicates novel pathways for the function of nuclear receptors and diverse mammalian activators

Composite co-activator ARC mediates chromatin-directed transcriptional activation

Mediator of Transcriptional Regulation

The Draft Genome of Ciona intestinalis: Insights into Chordate and Vertebrate Origins

Translating the Histone Code

The USA-derived transcriptional coactivator PC2 is a submodule of TRAP/SMCC and acts synergistically with other PCs

Selectivity of chromatin-remodelling cofactors for ligand-activated transcription

The TRAP/Mediator coactivator complex interacts directly with estrogen receptors alpha and beta through the TRAP220 subunit and directly enhances estrogen receptor function in vitro

Ligand induction of a transcriptionally active thyroid hormone receptor coactivator complex

Requirement of TRAP/mediator for both activator-independent and activator-dependent transcription in conjunction with TFIID-associated TAF(II)s.

P304

6494-504

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

4846851

http://www.w3.org/2001/XMLSchema#string

P356

10.1093/EMBOJ/CDG619

http://www.w3.org/2001/XMLSchema#string

P407

P433

24

http://www.w3.org/2001/XMLSchema#string

P478

22

http://www.w3.org/2001/XMLSchema#string

P50

Elisabeth Kremmer

P577

2003-12-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

8975030

http://www.w3.org/2001/XMLSchema#string

P698

14657022

http://www.w3.org/2001/XMLSchema#string

P932

291814

http://www.w3.org/2001/XMLSchema#string