The role of the C-terminal extension (CTE) of the estrogen receptor alpha and beta DNA binding domain in DNA binding and interaction with HMGB.
about
Structure of the progesterone receptor-deoxyribonucleic acid complex: novel interactions required for binding to half-site response elementsHigh mobility group protein 1: A collaborator in nucleosome dynamics and estrogen-responsive gene expressionHigh Mobility Group B Proteins, Their Partners, and Other Redox Sensors in Ovarian and Prostate CancerA progesterone receptor co-activator (JDP2) mediates activity through interaction with residues in the carboxyl-terminal extension of the DNA binding domainSteroid receptor coactivator-1 from brain physically interacts differentially with steroid receptor subtypesSteroid receptor coactivator-2 expression in brain and physical associations with steroid receptorsHMGB1: the jack-of-all-trades protein is a master DNA repair mechanic.Regulation of the amino-terminal transcription activation domain of progesterone receptor by a cofactor-induced protein folding mechanism.Amino acid function and docking site prediction through combining disease variants, structure alignments, sequence alignments, and molecular dynamics: a study of the HMG domain.HMGB1 in health and disease.Acetylation-mediated epigenetic regulation of glucocorticoid receptor activity: circadian rhythm-associated alterations of glucocorticoid actions in target tissuesAcetylation of estrogen receptor alpha by p300 at lysines 266 and 268 enhances the deoxyribonucleic acid binding and transactivation activities of the receptor.Expanding the paradigm for estrogen receptor binding and transcriptional activationStructural dynamics, intrinsic disorder, and allostery in nuclear receptors as transcription factors.Structural and functional analysis of domains of the progesterone receptor.Kaiso uses all three zinc fingers and adjacent sequence motifs for high affinity binding to sequence-specific and methyl-CpG DNA targets.High-mobility group box-1 in sterile inflammation.Effects of estradiol and 4-hydroxytamoxifen on the conformation, thermal stability, and DNA recognition of estrogen receptor beta.Genomic interaction between ER and HMGB2 identifies DDX18 as a novel driver of endocrine resistance in breast cancer cells.Mechanism of high-mobility group protein B enhancement of progesterone receptor sequence-specific DNA binding.Interaction of estrogen receptor alpha with proliferating cell nuclear antigen.
P2860
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P2860
The role of the C-terminal extension (CTE) of the estrogen receptor alpha and beta DNA binding domain in DNA binding and interaction with HMGB.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
The role of the C-terminal ext ...... ing and interaction with HMGB.
@en
type
label
The role of the C-terminal ext ...... ing and interaction with HMGB.
@en
prefLabel
The role of the C-terminal ext ...... ing and interaction with HMGB.
@en
P2093
P2860
P356
P1476
The role of the C-terminal ext ...... ding and interaction with HMGB
@en
P2093
Dean P Edwards
James S Adelman
Vida Senkus Melvin
W Lee Kraus
P2860
P304
14763-14771
P356
10.1074/JBC.M313335200
P407
P577
2004-01-21T00:00:00Z