Nucleosome disruption by human SWI/SNF is maintained in the absence of continued ATP hydrolysis. - Wikidata - awgldk - TriplyDB

Nucleosome disruption by human SWI/SNF is maintained in the absence of continued ATP hydrolysis.

Nucleosome disruption by human SWI/SNF is maintained in the absence of continued ATP hydrolysis.

http://www.wikidata.org/entity/Q38353891

about

Functional interactions between Sp1 or Sp3 and the helicase-like transcription factor mediate basal expression from the human plasminogen activator inhibitor-1 gene Purification and characterization of mSin3A-containing Brg1 and hBrm chromatin remodeling complexes Architectural DNA binding by a high-mobility-group/kinesin-like subunit in mammalian SWI/SNF-related complexes Distinct domains of erythroid Krüppel-like factor modulate chromatin remodeling and transactivation at the endogenous beta-globin gene promoter Octamer transfer and creation of stably remodeled nucleosomes by human SWI-SNF and its isolated ATPases High mobility group protein 1: A collaborator in nucleosome dynamics and estrogen-responsive gene expression Post-translational modifications of histones that influence nucleosome dynamics Rad26p regulates the occupancy of histone H2A-H2B dimer at the active genes in vivo Functional differences between the human ATP-dependent nucleosome remodeling proteins BRG1 and SNF2H MOT1-catalyzed TBP-DNA disruption: uncoupling DNA conformational change and role of upstream DNA ATP-dependent chromatin-remodeling complexes.The nucleosome remodeling complex, Snf/Swi, is required for the maintenance of transcription in vivo and is partially redundant with the histone acetyltransferase, Gcn5.ATP-dependent chromatin remodeling: going mobile.Using atomic force microscopy to study nucleosome remodeling on individual nucleosomal arrays in situ.Human SWI/SNF generates abundant, structurally altered dinucleosomes on polynucleosomal templates.Genetic lesions and perturbation of chromatin architecture: a road to cell transformation.Regulated nucleosome mobility and the histone code.Cooperative activity of BRG1 and Z-DNA formation in chromatin remodeling.ATP-dependent chromatin remodeling factors and their roles in affecting nucleosome fiber composition.Dynamic regulation of transcription factors by nucleosome remodeling Perturbation of nucleosome core structure by the SWI/SNF complex persists after its detachment, enhancing subsequent transcription factor binding.Chromatin remodeling complexes: ATP-dependent machines in action.Activation of RNA polymerase II by topologically linked DNA-tracking proteins.SNF2beta-BRG1 is essential for the viability of F9 murine embryonal carcinoma cells.Decoupling nucleosome recognition from DNA binding dramatically alters the properties of the Chd1 chromatin remodeler Human SWI/SNF drives sequence-directed repositioning of nucleosomes on C-myc promoter DNA minicircles Analysis of individual remodeled nucleosomes reveals decreased histone-DNA contacts created by hSWI/SNF.Stable remodeling of tailless nucleosomes by the human SWI-SNF complex SWI-SNF-mediated nucleosome remodeling: role of histone octamer mobility in the persistence of the remodeled state.ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor.Stability of a human SWI-SNF remodeled nucleosomal array.Direct imaging of human SWI/SNF-remodeled mono- and polynucleosomes by atomic force microscopy employing carbon nanotube tips.Fusions with histone H3 result in highly specific alteration of gene expression The SWI/SNF complex creates loop domains in DNA and polynucleosome arrays and can disrupt DNA-histone contacts within these domains.Nucleosome remodeling by the human SWI/SNF complex requires transient global disruption of histone-DNA interactions hSWI/SNF-catalyzed nucleosome sliding does not occur solely via a twist-diffusion mechanism.A model for chromatin remodeling by the SWI/SNF family.Distortion of histone octamer core promotes nucleosome mobilization by a chromatin remodeler.Catalytic activity of the yeast SWI/SNF complex on reconstituted nucleosome arrays.Mutations in both the structured domain and N-terminus of histone H2B bypass the requirement for Swi-Snf in yeast

P2860

Q22010204-D2D97F87-3A6A-4B6B-9D93-D41FE6E03DD1 Q24290894-CAA9E1BD-6C79-454D-82A7-9AE4AF0981B7 Q24321741-ADE8B563-4F38-4B82-9BDB-36D05972551B Q24538309-EFD24A64-33D9-46B9-8F03-4B7016E2BA39 Q24551966-9B8AD379-3020-4DFC-8C86-51EDE6205F41 Q26744313-1E5E8530-2918-4036-AD95-5A0641EB660A Q26852536-6E875835-E4F9-4F4B-8574-F1148BC1C206 Q27934015-982AE9E8-9A24-488F-96C4-47BE90B22B37 Q28204516-01A3DE79-7AEF-41E8-9E55-60F169260008 Q30307201-F6A589EE-B959-4EF3-BB45-C67F42A8BDD2 Q33786898-C43FF4F5-6ED9-4A40-9892-C3EE7048CA62 Q33891022-BF984F3F-E5EC-46AF-AD62-ADA6DD2AF875 Q33957135-FA999B93-DC9F-42F6-A651-E25C83AE1E26 Q34187149-9AC746E4-BD3E-4FDE-8409-F7E667714DE5 Q34230856-4B51AE6D-0955-460F-8FF4-8CFCD03D2C1E Q34349653-420BD2CD-6339-4117-A9A8-C3AFC4D7FF74 Q34364723-CA3DFE22-AB17-40D5-876C-E85779DB735E Q34520054-8E791887-2468-454B-BCCC-4BD19D90D8F9 Q35536023-8D5A011F-E655-46C3-9B8A-27E5C6C576DC Q35686044-5C9297CB-A28D-4233-A809-3308157B0EDB Q36060626-D3D98607-B9DE-4AD5-A254-ED481AD95F03 Q36226123-1DA9F758-996E-4502-8685-F1C22E0A8C09 Q36239308-7DA6391A-147B-446A-AC5E-D1ED736CE2E1 Q36573136-55F6DD89-D38E-4575-9FA0-F1C54AF20F93 Q36580964-57EC99EF-5287-4935-BDDC-B562275F54E7 Q36853031-1F5EE7CB-BD66-49B9-ABE7-B236F2BD6028 Q37384729-AA863E25-2A0F-464F-9885-E5B634B8FCE3 Q39444877-2F64F89A-A144-4DB3-99B5-20E57D0E65B3 Q39452532-FA669A0D-A9B2-45F6-9203-18A8EB49CACB Q39455992-73A0E9D7-3A6C-42D6-A73A-9FFAA6BB2715 Q39526775-2AF7CDE3-F441-4C18-BBA9-4FDB60995364 Q39529256-E95850E7-7D48-496A-85E2-5B52F30C58E0 Q39542293-597903A9-86BD-4290-9656-E8272298BA2D Q39611007-ACCB4BA6-E9D8-4E7A-82F9-7DB3397C7887 Q39674660-0614182C-7F78-415B-A182-FC7F29AA19CA Q39681649-14120DF1-A64F-41DD-97A7-7A018DE75E3F Q40945469-F8A64DBA-16FD-4370-BE9D-1BFAFD108327 Q42631191-113A4DB9-7C7C-4140-9A3C-457B93877165 Q42632600-B2EA27D8-36DE-467C-BF33-3566B8797FBC Q42664605-00474294-893F-48FB-A8A7-736BD4232F2B

P2860

Nucleosome disruption by human SWI/SNF is maintained in the absence of continued ATP hydrolysis.

http://www.wikidata.org/entity/Q38353891

description

1996 nî lūn-bûn

@nan

1996年の論文

@ja

1996年学术文章

@wuu

1996年学术文章

@zh-cn

1996年学术文章

@zh-hans

1996年学术文章

@zh-my

1996年学术文章

@zh-sg

1996年學術文章

@yue

1996年學術文章

@zh

1996年學術文章

@zh-hant

name

Nucleosome disruption by human ...... e of continued ATP hydrolysis.

@en

type

label

Nucleosome disruption by human ...... e of continued ATP hydrolysis.

@en

prefLabel

Nucleosome disruption by human ...... e of continued ATP hydrolysis.

@en

P1433

Q38353891-D3326721-FDF2-4C96-B3D4-0C8AB4A015BF

P1476

Q38353891-46F340DE-93F2-4429-AF0A-366D51E7C696

P2093

Q38353891-012AAB73-EFC9-4752-A4C9-8141F97DD778

Q38353891-C15F463C-4293-4B44-B5E6-25E8068F467C

Q38353891-C2F32F5B-1717-4DE7-AAA3-278C7ABE6C63

P2860

Q38353891-09F3FB9C-4004-4347-806F-D65B07C5BC77

Q38353891-0C29EEFF-91AE-4CC4-956E-2A8075113B7B

Q38353891-1109F3FA-8152-4889-B72F-311F4302BF72

Q38353891-13D302D3-7D82-4D24-9E9F-177C3DE4706F

Q38353891-14694750-3EBD-459B-A49A-B4AC1841AC35

Q38353891-192CB351-3B12-4C33-A141-1AD78086A409

Q38353891-28777323-C679-4648-B60E-03847AFB844A

Q38353891-3205445B-444C-470F-82E5-D699285FC064

Q38353891-3507E1E7-FFC9-469B-85C9-F03F48F28F86

Q38353891-35BF3D64-14A8-4890-A1F1-346FEA82D967

P304

Q38353891-4E95C84C-910D-4D5F-9D90-BE75793588EF

P31

Q38353891-158A6541-BA2E-46B2-9323-0ECFF5F3A367

P356

Q38353891-9A391F8A-3819-4D4F-A8D1-A50885AD94DB

P407

Q38353891-A84C221D-8633-43CD-B121-7DFB6D2207AF

P433

Q38353891-898D7885-DF99-43F6-B866-4F6F75ADA38B

P478

Q38353891-B000FDDB-F37E-4237-9161-E8C18CC7370F

P577

Q38353891-2D91FB9D-F73C-4FF5-A9DC-BD60CFF6CB8B

P698

Q38353891-62B5A777-BD93-4008-A373-89223336D859

P356

JBC.271.34.20726

P1433

Journal of Biological Chemistry

P1476

Nucleosome disruption by human ...... e of continued ATP hydrolysis.

@en

P2093

Imbalzano AN

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

Kingston RE

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

Schnitzler GR

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

P2860

Two human homologues of Saccharomyces cerevisiae SWI2/SNF2 and Drosophila brahma are transcriptional coactivators cooperating with the estrogen receptor and the retinoic acid receptor

BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription

The retinoblastoma protein and BRG1 form a complex and cooperate to induce cell cycle arrest

Binding and stimulation of HIV-1 integrase by a human homolog of yeast transcription factor SNF5

The SNF5 protein of Saccharomyces cerevisiae is a glutamine- and proline-rich transcriptional activator that affects expression of a broad spectrum of genes.

Five SWI/SNF gene products are components of a large multisubunit complex required for transcriptional enhancement.

Characterization of the yeast SWI1, SWI2, and SWI3 genes, which encode a global activator of transcription.

A negative regulator of HO transcription, SIN1 (SPT2), is a nonspecific DNA-binding protein related to HMG1.

Functional interdependence of the yeast SNF2, SNF5, and SNF6 proteins in transcriptional activation.

Stimulation of GAL4 derivative binding to nucleosomal DNA by the yeast SWI/SNF complex

P304

20726-20733

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

P31

scholarly article

P356

10.1074/JBC.271.34.20726

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

P407

P433

34

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

P478

271

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

P577

1996-08-01T00:00:00Z

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

P698

8702824

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