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The MTA1 (show MTA1 Proteins) subunit of the nucleosome remodeling and deacetylase complex can recruit two copies of RBBP4 (show RBBP4 Proteins)/RBBP7 (show RBBP7 Proteins).
RbAp48 (show RBBP4 Proteins) is likely to act as a potent antiretroviral defense.
The crystal structure reveals an extensive interface between MTA1 (show MTA1 Proteins) and RBBP4 (show RBBP4 Proteins).
RBBP4 (show RBBP4 Proteins) interacts with ep300 (show EP300 Proteins) protein to form a complex that drives the expression of methylguanine-DNA-methyltransferase (show MGMT Proteins) , RAD51 (show RAD51 Proteins), and other selected DNA repair genes through histone acetylation.
RbAp48 (show RBBP4 Proteins) was identified as critical in the proliferation of hypopharyngeal carcinoma in both in vitro and in vivo experiments.
RBBP4 functions as a novel regulatory factor to increase the efficiency of importin alpha/beta-mediated nuclear import
Our RBBP4 (show RBBP4 Proteins)-PHF6 (show PHF6 Proteins) complex structure provides insights into the molecular basis of PHF6 (show PHF6 Proteins)-NuRD complex interaction and implicates a role for PHF6 (show PHF6 Proteins) in chromatin structure modulation and gene regulation.
Our results reveal that the protein structure does not affect ligand binding, and the top three TCM candidates Bittersweet alkaloid II, Eicosandioic acid, and Perivine might resolve the instability of the RbAp48 (show RBBP4 Proteins)-FOG1 (show ZFPM1 Proteins) complex
RbAp48 (show RBBP4 Proteins) recognizes MTA1 (show MTA1 Proteins) using the same site that it uses to bind histone H4, showing that assembly into NuRD modulates RbAp46 (show RBBP7 Proteins)/48 interactions with histones.
The most significant change was an age-related decline in RbAp48 (show RBBP4 Proteins), a histone-binding protein that modifies histone acetylation.
RBBP4 (show RBBP4 Proteins) is a regulator of histone deacetylation during oocyte maturation and deacetylation is required for bipolar spindle assembly through Aurora kinase C (show AURKC Proteins)
Studies indicate that estrogen deficiency initiates tissue-specific apoptosis in the exocrine gland cells through RbAp48 (show RBBP4 Proteins) overexpression.
Estrogen deficiency initiates p53 (show TP53 Proteins)-mediated apoptosis in the exocrine glands through Rbbp4 (show RBBP4 Proteins) overexpression.
Results report that transgenic expression of RbAp48 (show RBBP4 Proteins) resulted in the development of autoimmune exocrinopathy resembling Sjogren's syndrome.
This gene encodes a ubiquitously expressed nuclear protein which belongs to a highly conserved subfamily of WD-repeat proteins. It is present in protein complexes involved in histone acetylation and chromatin assembly. It is part of the Mi-2 complex which has been implicated in chromatin remodeling and transcriptional repression associated with histone deacetylation. This encoded protein is also part of co-repressor complexes, which is an integral component of transcriptional silencing. It is found among several cellular proteins that bind directly to retinoblastoma protein to regulate cell proliferation. This protein also seems to be involved in transcriptional repression of E2F-responsive genes. Three transcript variants encoding different isoforms have been found for this gene.
, histone-binding protein RBBP4
, nucleosome-remodeling factor subunit RBAP48
, retinoblastoma-binding protein 4
, CAF-1 subunit C
, CAF-I 48 kDa subunit
, CAF-I p48
, chCAF-1 p48
, chromatin assembly factor 1 p48 subunit
, chromatin assembly factor 1 subunit C
, chromatin assembly factor I p48 subunit
, retinoblastoma-binding protein p48
, MSI1 protein homolog
, chromatin assembly factor/CAF-1 p48 subunit
, CAF-1 p48 subunit
, histone-binding protein RBBP4-A
, retinoblastoma A associated protein
, retinoblastoma-binding protein 4-A
, retinoblastoma-binding protein p48-A